DPYD NM_000110.4:c.1236G>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1236 of the coding sequence of the DPYD gene where guanine has been mutated to adenine.

**Synonyms:** - DHP c.1236G>A - DHPDHASE c.1236G>A - DPD c.1236G>A - DPYD Polymorphism rs56038477 - DPYD c.1236G>A - Dihydropyrimidine Dehydrogenase c.1236G>A - NM_000110.4:c.1236G>A