IDH2 NM_002168.3:c.418C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 418 of the coding sequence of the IDH2 gene where cytosine has been mutated to thymine.

**Synonyms:** - IDH c.418C>T - IDH2 c.418C>T - Isocitrate Dehydrogenase (NADP(+)) 2, Mitochondrial c.418C>T - Isocitrate Dehydrogenase 2 (NADP+), Mitochondrial c.418C>T - NM_002168.3:c.418C>T