Canonical Allele Identifier: PA2741901428
Gene: VIM HGNC NCBI

Linked Data

ClinVar Variation Id: 2872982
ClinVar RCV Id: RCV003742422
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003371.2:p.Arg28Gly
CA376174915
NM_003380.5:c.82C>G