Allele Registry

Canonical Allele Identifier: PA2573063445

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086830

RCV000343743

RCV000826083

RCV002243746

RCV004549531

ClinVar Variation:

100420

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ser1731Thr	CA228704 NM_000552.5:c.5191T>A