Allele Registry

Canonical Allele Identifier: PA3057313939

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV004821401

ClinVar Variation:

3393379

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ala1714Pro	CA383496428 NM_000552.5:c.5140G>C