Allele Registry

Canonical Allele Identifier: PA2573063290

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000000339

RCV000086691

ClinVar Variation:

311

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ser1285Phe	CA114164 NM_000552.5:c.3854C>T