FGFR2 NM_000141.4:c.1647T>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1647 of the coding sequence of the FGFR2 gene where thymine has been mutated to adenine.

**Synonyms:** - BEK c.1647T>A - CD332 c.1647T>A - ECT1 c.1647T>A - FGFR2 c.1647T>A - Fibroblast Growth Factor Receptor 2 c.1647T>A - K-SAM c.1647T>A - KGFR c.1647T>A - NM_000141.4:c.1647T>A