Canonical Allele Identifier: PA916022175
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Thr79Met
CA160026
NM_001318054.2:c.236C>T