Canonical Allele Identifier: PA2741898222
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2749982
ClinVar RCV Id: RCV003540268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Lys135Arg
CA1020714
NM_002524.5:c.404A>G