Canonical Allele Identifier: PA658676122
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 462156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Pro173Leu
CA378921066
NM_005343.4:c.518C>T