Canonical Allele Identifier: PA129949
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly12Cys
CA129948
NM_005343.4:c.34G>T