Canonical Allele Identifier: PA2829601143
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2416982
ClinVar RCV Id: RCV003111810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ile163Met
CA378921153
NM_005343.4:c.489C>G