NRAS NM_002524.5:c.38G>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 38 of the coding sequence of the NRAS gene where guanine has been mutated to adenine.

**Synonyms:** - N-ras c.38G>A - NM_002524.5:c.38G>A - NRAS c.38G>A - NRAS1 c.38G>A - Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.38G>A