EGFR NP_005219.2:p.S768X

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A change in the amino acid residue at position 768 in the epidermal growth factor receptor protein where serine has been replaced by another amino acid.

**Synonyms:** - EGFR NP_005219.2:p.Ser768Xxx - EGFR S768X - EGFR S768X Mutation - EGFR Ser768Xxx - EGFR p.S768X - EGFR p.Ser768Xxx - Epidermal Growth Factor Receptor S768X - Epidermal Growth Factor Receptor Ser768Xxx - NP_005219.2:p.S768X - NP_005219.2:p.Ser768Xxx - Proto-Oncogene c-ErbB-1 S768X - Proto-Oncogene c-ErbB-1 Ser768Xxx - Receptor Tyrosine-Protein Kinase erbB-1 S768X - Receptor Tyrosine-Protein Kinase erbB-1 Ser768Xxx