PDGFRA NM_006206.6:c.1682T>A

**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 adenine

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