Allele Registry

Canonical Allele Identifier: PA2573063409

Gene: VWF HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

15349

ClinVar RCV:

RCV000000338

RCV000086795

RCV000622977

RCV000678772

RCV001255177

RCV001843449

RCV002280857

RCV003313770

RCV004547448

ClinVar Variation:

310

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Tyr1584Cys	CA114162 NM_000552.5:c.4751A>G