DRD2 NM_000795.3:c.957C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 957 of the coding sequence of the DRD2 gene where cytosine has been mutated to thymine.

**Synonyms:** - DRD2 957T Indel Mutation - DRD2 C957T Indel Mutation - DRD2 c.957C>T - Dopamine Receptor D2 c.957C>T - NM_000795.3:c.957C>T