Allele Registry

Canonical Allele Identifier: PA2573063064

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000760113

RCV000765104

RCV000852047

RCV002264696

RCV003147455

RCV003323534

RCV004551444

ClinVar Variation:

381621

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ala542Gly	CA6403319 NM_000552.5:c.1625C>G