Canonical Allele Identifier: PA106170
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13903
ClinVar RCV Id: RCV000014917 RCV000158982 RCV000208552 RCV001382056 RCV003415702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly60Glu
CA257021
NM_002524.5:c.179G>A