Canonical Allele Identifier: PA2579930989
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 180849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg68Gln
CA296059
NM_001130442.3:c.203G>A