PDGFRA NM_006206.6:c.1729C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1729 of the coding sequence of the PDGFRA gene where cytosine has been mutated to thymine.

**Synonyms:** - CD140A c.1729C>T - NM_006206.6:c.1729C>T - PDGFR-2 c.1729C>T - PDGFR2 c.1729C>T - PDGFRA c.1729C>T - Platelet-Derived Growth Factor Receptor, Alpha Polypeptide c.1729C>T - RHEPDGFRA c.1729C>T