C177473Level 5
EGFR NP_005219.2:p.V774M
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the amino acid residue at position 774 in the epidermal growth factor receptor protein where valine has been replaced by methionine.
**Synonyms:** - Activating V774M Mutation - EGFR NP_005219.2:p.Val774Met - EGFR V774M - EGFR V774M Mutation - EGFR Val774Met - EGFR p.V774M - EGFR p.Val774Met - Epidermal Growth Factor Receptor V774M - Epidermal Growth Factor Receptor Val774Met - NP_005219.2:p.V774M - NP_005219.2:p.Val774Met - Proto-Oncogene c-ErbB-1 V774M - Proto-Oncogene c-ErbB-1 Val774Met - Receptor Tyrosine-Protein Kinase erbB-1 V774M - Receptor Tyrosine-Protein Kinase erbB-1 Val774Met
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