Canonical Allele Identifier: PA2829600857
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1021434
ClinVar RCV Id: RCV001321198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg68Leu
CA378924629
NM_005343.4:c.203G>T