Allele Registry

Canonical Allele Identifier: PA2573063315

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086718

RCV002222015

RCV002243734

ClinVar Variation:

100314

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Pro1337Leu	CA228510 NM_000552.5:c.4010C>T