APC NM_000038.6:c.3920T>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 3920 of the coding sequence of the APC gene where adenine has been mutated to thymine.

**Synonyms:** - APC c.3920T>A - APC, WNT Signaling Pathway Regulator c.3920T>A - Adenomatosis Polyposis Gene c.3920T>A - BTPS2 c.3920T>A - FAP c.3920T>A - FPC c.3920T>A - NM_000038.6:c.3920T>A - PPP1R46 c.3920T>A