EGFR NP_005219.2:p.M766_A767insASV
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** An insertion of the amino acid sequence alanine-serine-valine between the methionine at position 766 and the alanine at position 767 of the epidermal growth factor receptor protein.
**Synonyms:** - EGFR M766_A767insASV - EGFR Met766_Ala767insAlaSerVal - EGFR NP_005219.2:p.Met766_Ala767insAlaSerVal - EGFR p.M766_A767insASV - EGFR p.Met766_Ala767insAlaSerVal - Epidermal Growth Factor Receptor M766_A767insASV - Epidermal Growth Factor Receptor Met766_Ala767insAlaSerVal - NP_005219.2:p.M766_A767insASV - NP_005219.2:p.Met766_Ala767insAlaSerVal - Proto-Oncogene c-ErbB-1 M766_A767insASV - Proto-Oncogene c-ErbB-1 Met766_Ala767insAlaSerVal - Receptor Tyrosine-Protein Kinase erbB-1 Met766_Ala767insAlaSerVal
/api/v1/systems/nci_thesaurus/nodes/C138903Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.