NRAS NM_002524.4:c.37G>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 37 of the coding sequence of the NRAS gene where guanine has been mutated to cytosine.

**Synonyms:** - N-ras c.37G>C - NM_002524.4:c.37G>C - NRAS G13R (c.37G>C) mutation - NRAS c.37G>C - NRAS1 c.37G>C - Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.37G>C