NRAS NM_002524.4:c.37G>A

**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 adenine.

**Synonyms:** - N-ras c.37G>A - NM_002524.4:c.37G>A - NRAS G13S (c.37G>A) mutation - NRAS c.37G>A - NRAS1 c.37G>A - Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.37G>A