Allele Registry

Canonical Allele Identifier: PA2573063248

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086649

RCV000851636

RCV002281057

ClinVar Variation:

100256

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Trp1120Ser	CA228396 NM_000552.5:c.3359G>C