Homo sapiens von Willebrand factor A domain containing 1 (VWA1), trans - Nucleotide

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Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy. [Brain. 2021]
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
Pagnamenta AT, Kaiyrzhanov R, Zou Y, Da'as SI, Maroofian R, Donkervoort S, Dominik N, Lauffer M, Ferla MP, Orioli A, et al. Brain. 2021 Mar 3; 144(2):584-600.
Bi-allelic truncating mutations in VWA1 cause neuromyopathy. [Brain. 2021]
Bi-allelic truncating mutations in VWA1 cause neuromyopathy.
Deschauer M, Hengel H, Rupprich K, Kreiß M, Schlotter-Weigel B, Grimmel M, Admard J, Schneider I, Alhaddad B, Gazou A, et al. Brain. 2021 Mar 3; 144(2):574-583.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the VWA1 gene (NM_199121.3).
RefSeq protein product
See the reference protein sequence for von Willebrand factor A domain-containing protein 1 isoform 1 precursor (NP_073745.2).

Protein
Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Nucleotide