Canonical Allele Identifier: PA915998571
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 812886
ClinVar RCV Id: RCV001003789 RCV001261065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Ala59Asp
CA341741639
NM_002524.5:c.176C>A