C98446Level 7
NRAS NM_002524.4:c.181C>A
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A nucleotide substitution at position 181 of the coding sequence of the NRAS gene where cytosine has been mutated to adenine.
**Synonyms:** - N-ras c.181C>A - NM_002524.4:c.181C>A - NRAS Q61K (c.181C>A) mutation - NRAS c.181C>A - NRAS1 c.181C>A - Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.181C>A
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Cross-system equivalences0
No cross-system equivalences mapped for this node.