Allele Registry

Canonical Allele Identifier: PA2573063298

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086706

RCV000678766

RCV002243731

ClinVar Variation:

100305

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ile1309Val	CA228492 NM_000552.5:c.3925A>G