Allele Registry

Canonical Allele Identifier: PA2573063390

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086782

RCV002222391

ClinVar Variation:

100376

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ser1543Phe	CA228628 NM_000552.5:c.4628C>T