Allele Registry

Canonical Allele Identifier: PA2573063117

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086746

ClinVar Variation:

100341

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Asp141Gly	CA228563 NM_000552.5:c.422A>G