Canonical Allele Identifier: PA645475150
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly12Arg
CA16602439
NM_005343.4:c.34G>C