C163752Level 5
EGFR NP_005219.2:p.V769L
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the amino acid residue at position 769 in the epidermal growth factor receptor protein where valine has been replaced by leucine.
**Synonyms:** - EGFR NP_005219.2:p.Val769Leu - EGFR V769L - EGFR V769L Mutation - EGFR Val769Leu - EGFR p.V769L - EGFR p.Val769Leu - Epidermal Growth Factor Receptor V769L - Epidermal Growth Factor Receptor Val769Leu - NP_005219.2:p.V769L - NP_005219.2:p.Val769Leu - Proto-Oncogene c-ErbB-1 V769L - Proto-Oncogene c-ErbB-1 Val769Leu - Receptor Tyrosine-Protein Kinase erbB-1 V769L - Receptor Tyrosine-Protein Kinase erbB-1 Val769Leu
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