Allele Registry

Canonical Allele Identifier: PA2573063506

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086863

RCV001787069

RCV002264669

ClinVar Variation:

100451

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Cys2304Tyr	CA228762 NM_000552.5:c.6911G>A