NM_000271.5(NPC1):c.387_388inv (p.Val130Ile) AND Niemann-Pick disease, type C1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001952439.3
Allele description [Variation Report for NM_000271.5(NPC1):c.387_388inv (p.Val130Ile)]
NM_000271.5(NPC1):c.387_388inv (p.Val130Ile)
Condition(s)
- Name:
- Niemann-Pick disease, type C1
- Synonyms:
- NIEMANN-PICK DISEASE WITHOUT SPHINGOMYELINASE DEFICIENCY; Niemann-Pick disease with cholesterol esterification block; Niemann-Pick disease, chronic neuronopathic form; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009757; MedGen: C3179455; Orphanet: 646; OMIM: 257220
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KSU-FBSSR-6S Vicia faba Giza 716 SSR enriched library Vicia faba genomic clone K...
KSU-FBSSR-6S Vicia faba Giza 716 SSR enriched library Vicia faba genomic clone KSU-FBSSR-6S, genomic survey sequencegi|392283814|gnl|dbGSS|34677988|gb| 335.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024