Canonical Allele Identifier: PA2829600858
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1062564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg68Gly
CA378924632
NM_005343.4:c.202C>G