Canonical Allele Identifier: PA2580278777
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2054868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ser87Cys
CA341741403
NM_002524.5:c.259A>T