C98574Level 5
EGFR NP_005219.2:p.T751_E758del
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A deletion of eight amino acids from the epidermal growth factor receptor protein from the threonine at position 751 through the glutamic acid at position 758.
**Synonyms:** - EGFR NP_005219.2:p.Thr751_Glu758del - EGFR T751_E758 Deletion Mutation - EGFR T751_E758del - EGFR p.T751_E758del - Epidermal Growth Factor Receptor T751_E758del - NP_005219.2:p.T751_E758del - NP_005219.2:p.Thr751_Glu758del - Proto-Oncogene c-ErbB-1 T751_E758del - Receptor Tyrosine-Protein Kinase erbB-1 T751_E758del
GET
/api/v1/systems/nci_thesaurus/nodes/C98574Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.