C98553Level 5
EGFR NP_005219.2:p.L747_A755del
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A deletion of nine amino acids from the epidermal growth factor receptor protein from the leucine at position 747 through the alanine at position 755.
**Synonyms:** - EGFR L747_A755 Deletion Mutation - EGFR L747_A755del - EGFR NP_005219.2:p.Leu747_Ala755del - EGFR p.L747_A755del - Epidermal Growth Factor Receptor L747_A755del - NP_005219.2:p.Leu747_Ala755del - Proto-Oncogene c-ErbB-1 L747_A755del - Receptor Tyrosine-Protein Kinase erbB-1 L747_A755del
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