EGFR NP_005219.2:p.R748_S752del

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A deletion of five amino acids from the epidermal growth factor receptor protein from the arginine at position 748 through the serine at position 752.

**Synonyms:** - EGFR NP_005219.2:p.Arg748_Ser752del - EGFR R748_S752 Deletion Mutation - EGFR R748_S752del - EGFR p.R748_S752del - Epidermal Growth Factor Receptor R748_S752del - NP_005219.2:p.Arg748_Ser752del - Proto-Oncogene c-ErbB-1 R748_S752del - Receptor Tyrosine-Protein Kinase erbB-1 R748_S752del