Allele Registry

Canonical Allele Identifier: PA2573063335

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086736

RCV002243737

RCV002264659

ClinVar Variation:

100331

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1374Leu	CA228543 NM_000552.5:c.4121G>T