Canonical Allele Identifier: PA2573063269
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100273
ClinVar RCV Id: RCV000086669 RCV001787055
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys1227Arg
CA228431
NM_000552.5:c.3679T>C