Allele Registry

Canonical Allele Identifier: PA2573063192

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000024003

RCV000086595

ClinVar Variation:

31011

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg760His	CA228316 NM_000552.5:c.2279G>A