EGFR NP_005219.2:p.S752_V769del

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A deletion of 18 amino acids from the epidermal growth factor receptor protein from the serine at position 752 through the valine at position 769.

**Synonyms:** - EGFR NP_005219.2:p.Ser752_Val769del - EGFR S752_V769 Deletion Mutation - EGFR S752_V769del - EGFR p.S752_V769del - Epidermal Growth Factor Receptor S752_V769del - NP_005219.2:p.S752_V769del - NP_005219.2:p.Ser752_Val769del - Proto-Oncogene c-ErbB-1 S752_V769del - Receptor Tyrosine-Protein Kinase erbB-1 S752_V769del