Allele Registry

Canonical Allele Identifier: PA2580118628

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV002280977

ClinVar Variation:

1703818

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Val1316Leu	CA6402646 NM_000552.5:c.3946G>C CA383506089 NM_000552.5:c.3946G>T