Allele Registry

Canonical Allele Identifier: PA2573063506

Gene: VWF HGNC NCBI

ClinVar Variation Id: 100451

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Cys2304Tyr	CA228762 NM_000552.5:c.6911G>A