Allele Registry

Canonical Allele Identifier: PA2573063153

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000249735

RCV000390452

RCV001357216

RCV002243949

RCV002243950

RCV002243951

ClinVar Variation:

256654

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.His484Arg	CA6403395 NM_000552.5:c.1451A>G