C223121Level 5
EGFR NP_005219.2:p.L747X
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the amino acid residue at position 747 in the epidermal growth factor receptor protein where leucine has been replaced by another amino acid.
**Synonyms:** - EGFR L747X - EGFR L747X Mutation - EGFR Leu747Xxx - EGFR NP_005219.2:p.Leu747Xxx - EGFR p.L747X - EGFR p.Leu747Xxx - Epidermal Growth Factor Receptor L747X - Epidermal Growth Factor Receptor Leu747Xxx - NP_005219.2:p.L747X - NP_005219.2:p.Leu747Xxx - Proto-Oncogene c-ErbB-1 L747X - Proto-Oncogene c-ErbB-1 Leu747Xxx - Receptor Tyrosine-Protein Kinase erbB-1 L747X - Receptor Tyrosine-Protein Kinase erbB-1 Leu747Xxx
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