Canonical Allele Identifier: PA2573063570
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100499
ClinVar RCV Id: RCV000086913
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2754Trp
CA228840
NM_000552.5:c.8262T>G