Canonical Allele Identifier: PA2580278781
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2284381
ClinVar RCV Id: RCV004138465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Tyr137Cys
CA341739206
NM_002524.5:c.410A>G