EGFR NP_005219.2:p.L747_S752del

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A deletion of six amino acids from the epidermal growth factor receptor protein from the leucine at position 747 through the serine at position 752.

**Synonyms:** - EGFR L747_S752 Deletion Mutation - EGFR L747_S752del - EGFR NP_005219.2:p.Leu747_Ser752delLeuArgGluAlaThrSer - EGFR p.L747_S752del - Epidermal Growth Factor Receptor L747_S752del - NP_005219.2:p.Leu747_Ser752delLeuArgGluAlaThrSer - Proto-Oncogene c-ErbB-1 L747_S752del - Receptor Tyrosine-Protein Kinase erbB-1 L747_S752del