Canonical Allele Identifier: PA2829601136
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1034833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Glu162Lys
CA378921167
NM_005343.4:c.484G>A