Allele Registry

Canonical Allele Identifier: PA2573063412

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086796

ClinVar Variation:

100389

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1597Gly	CA228653 NM_000552.5:c.4789C>G