Canonical Allele Identifier: PA658830290
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 561731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ile46Thr
CA378924769
NM_005343.4:c.137T>C