Canonical Allele Identifier: PA2829601153
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1019189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.His166Arg
CA378921139
NM_005343.4:c.497A>G