Allele Registry

Canonical Allele Identifier: PA2573063086

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086752

RCV002243741

ClinVar Variation:

100347

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ala1437Thr	CA228575 NM_000552.5:c.4309G>A