C98561Level 5
EGFR NP_005219.2:p.L747_T751del
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A deletion of five amino acids from the epidermal growth factor receptor protein from the leucine at position 747 through the threonine at position 751.
**Synonyms:** - EGFR L747_T751 Deletion Mutation - EGFR L747_T751del - EGFR NP_005219.2:p.Leu747_Thr751del - EGFR p.L747_T751del - Epidermal Growth Factor Receptor L747_T751del - NP_005219.2:p.Leu747_Thr751del - Proto-Oncogene c-ErbB-1 L747_T751del - Receptor Tyrosine-Protein Kinase erbB-1 L747_T751del
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