Allele Registry

Canonical Allele Identifier: PA2573063448

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086832

RCV000852150

RCV001001933

RCV004549532

ClinVar Variation:

100422

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Val1760Ile	CA228708 NM_000552.5:c.5278G>A