Canonical Allele Identifier: PA2829408033
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 3222657
ClinVar RCV Id: RCV004516041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ala91Gly
CA341741336
NM_002524.5:c.272C>G