Canonical Allele Identifier: PA2829600763
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2763385
ClinVar RCV Id: RCV003515838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg41Gln
CA378924802
NM_005343.4:c.122G>A