Allele Registry

Canonical Allele Identifier: PA2573063330

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086731

RCV000851784

RCV002222390

ClinVar Variation:

100326

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Phe1369Ile	CA228533 NM_000552.5:c.4105T>A