Canonical Allele Identifier: PA2573063586
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100509
ClinVar RCV Id: RCV000086924
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2806Arg
CA228858
NM_000552.5:c.8416T>C