Canonical Allele Identifier: PA1139709530
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 933172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Arg68Thr
CA341741583
NM_002524.5:c.203G>C