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Accession: PRJEB56309 ID: 886588

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First observation of a mutation (L26F) in a weak D phenotype encoded by 76 C>T, ethnic origin: Austria

Sanger sequencing of RHD exons 1 to 10 and boundaries elucidated a novel C>T alteration at position 76 causing for a L26F amino acid alteration. More...

Accession	PRJEB56309
Scope	Monoisolate
Submission	Registration date: 3-Oct-2022 RED CROSS TRANSFUSION SERVICE FOR UPPER AUSTRIA

Project Data:

Resource Name	Number of Links
Sequence data
Nucleotide (Genomic DNA)	1
Protein Sequences	1

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First observation of a mutation (L26F) in a weak D phenotype encoded by 76 C>T, ethnic origin: Austria

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