EGFR NP_005219.2:p.S768I

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the amino acid residue at position 768 in the epidermal growth factor receptor protein where serine has been replaced by isoleucine.

**Synonyms:** - Activating S768I Mutation - EGFR Exon 20 S768I - EGFR NP_005219.2:p.Ser768Ile - EGFR S768I - EGFR S768I Mutation - EGFR Ser768Ile - EGFR p.S768I - EGFR p.Ser768Ile - Epidermal Growth Factor Receptor S768I - NP_005219.2:p.Ser768Ile - Proto-Oncogene c-ErbB-1 S768I - Receptor Tyrosine-Protein Kinase erbB-1 S768I