Canonical Allele Identifier: PA658807711
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 517437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg161His
CA5779221
NM_005343.4:c.482G>A