C223881Level 7
PDGFRA NM_006206.6:c.1696_1713del
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A deletion of 18 nucleotides from the coding sequence of the PDGFRA gene from position 1696 through 1713.
**Synonyms:** - CD140A c.1696_1713del - NM_006206.6:c.1696_1713del - PDGFR-2 c.1696_1713del - PDGFR2 c.1696_1713del - PDGFRA c.1696_1713del - PDGFRA c.1696_1713del18 - PDGFRA c.1696_1713delAGCCCAGATGGACATGAA - Platelet-Derived Growth Factor Receptor, Alpha Polypeptide c.1696_1713del - RHEPDGFRA c.1696_1713del
GET
/api/v1/systems/nci_thesaurus/nodes/C223881Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.