C98566Level 5
EGFR NP_005219.2:p.R748_P753del
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A deletion of six amino acids from the epidermal growth factor receptor protein from the arginine at position 748 through the proline at position 753.
**Synonyms:** - EGFR NP_005219.2:p.Arg748_Pro753del - EGFR R748_P753 Deletion Mutation - EGFR R748_P753del - EGFR p.R748_P753del - Epidermal Growth Factor Receptor R748_P753del - NP_005219.2:p.Arg748_Pro753del - Proto-Oncogene c-ErbB-1 R748_P753del - Receptor Tyrosine-Protein Kinase erbB-1 R748_P753del
GET
/api/v1/systems/nci_thesaurus/nodes/C98566Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.