Allele Registry

Canonical Allele Identifier: PA2573063277

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086678

RCV002243726

RCV002243727

ClinVar Variation:

100281

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.His1268Asp	CA228445 NM_000552.5:c.3802C>G