Canonical Allele Identifier: PA2573081995
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1320232
ClinVar RCV Id: RCV001775405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gln150Arg
CA341739009
NM_002524.5:c.449A>G