DPYD NM_000110.3:c.1627A>G

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1627 of the coding sequence of the DPYD gene where adenine has been mutated to guanine.

**Synonyms:** - DHP c.1627A>G - DHPDHASE c.1627A>G - DPD c.1627A>G - DPYD c.1627A>G - Dihydropyrimidine Dehydrogenase c.1627A>G - NM_000110.3:c.1627A>G