Allele Registry

Canonical Allele Identifier: PA2573063327

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086728

RCV000678768

RCV000851781

ClinVar Variation:

100323

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Leu1361Ser	CA228528 NM_000552.5:c.4082T>C