Allele Registry

Canonical Allele Identifier: PA2573063341

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000251458

RCV000337059

RCV001354682

RCV002244013

RCV002244014

RCV002244015

ClinVar Variation:

256678

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Thr1381Ala	CA6402593 NM_000552.5:c.4141A>G