Canonical Allele Identifier: PA2573063576
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 306
ClinVar RCV Id: RCV000000333 RCV000086917
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2773Arg
CA114158
NM_000552.5:c.8317T>C