PDGFRA NM_006206.6:c.1682T>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1682 of the coding sequence of the PDGFRA gene where thymine has been mutated to cytosine.

**Synonyms:** - CD140A c.1682T>C - NM_006206.6:c.1682T>C - PDGFR-2 c.1682T>C - PDGFR2 c.1682T>C - PDGFRA c.1682T>C - Platelet-Derived Growth Factor Receptor, Alpha Polypeptide c.1682T>C - RHEPDGFRA c.1682T>C