Allele Registry

Canonical Allele Identifier: PA2573063496

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086855

RCV000241790

RCV000401548

RCV002243751

RCV002243752

RCV002243753

RCV002483170

ClinVar Variation:

100443

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg2185Gln	CA228748 NM_000552.5:c.6554G>A