C98577Level 5
EGFR NP_005219.2:p.S752_I759del
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A deletion of eight amino acids from the epidermal growth factor receptor protein from the serine at position 752 through the isoleucine at position 759.
**Synonyms:** - EGFR NP_005219.2:p.Ser752_Ile759delSerProLysAlaAsnLysGluIle - EGFR S752_I759 Deletion Mutation - EGFR S752_I759del - EGFR p.S752_I759del - Epidermal Growth Factor Receptor S752_I759del - NP_005219.2:p.S752_I759del - NP_005219.2:p.Ser752_Ile759delSerProLysAlaAsnLysGluIle - Proto-Oncogene c-ErbB-1 S752_I759del - Receptor Tyrosine-Protein Kinase erbB-1 S752_I759del
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Cross-system equivalences0
No cross-system equivalences mapped for this node.