NRAS NM_002524.4:c.182A>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 182 of the coding sequence of the NRAS gene where adenine has been mutated to thymine.

**Synonyms:** - N-ras c.182A>T - NM_002524.4:c.182A>T - NRAS Q61L (c.182A>T) mutation - NRAS c.182A>T - NRAS1 c.182A>T - Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.182A>T