Allele Registry

Canonical Allele Identifier: PA2573063558

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086902

RCV001787081

ClinVar Variation:

100488

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Cys2671Tyr	CA228821 NM_000552.5:c.8012G>A