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C98672Level 5

EGFR NP_005219.2:p.N771_P772insN

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** An insertion of the amino acid asparagine between the asparagine at position 771 and the proline at position 772 of the epidermal growth factor receptor protein.

**Synonyms:** - EGFR N771 Duplication Mutation - EGFR N771_P772insN - EGFR NP_005219.2:p.Asn771_Pro772insAsn - EGFR NP_005219.2:p.N771dup - EGFR p.N771_P772insN - Epidermal Growth Factor Receptor N771_P772insN - NP_005219.2:p.Asn771dup - NP_005219.2:p.N771_P772insN - NP_005219.2:p.N771dup - Proto-Oncogene c-ErbB-1 N771_P772insN - Receptor Tyrosine-Protein Kinase erbB-1 N771_P772insN

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