Allele Registry

Canonical Allele Identifier: PA2573063451

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086833

RCV000852152

ClinVar Variation:

100423

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Leu1774Ser	CA228710 NM_000552.5:c.5321T>C