ERBB2 NP_004439.2:p.I767M

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the amino acid residue at position 767 in the receptor tyrosine-protein kinase erbB-2 protein where isoleucine has been replaced by methionine.

**Synonyms:** - Activating I767M Mutation - ERBB2 I767M - ERBB2 Ile767Met - ERBB2 NP_004439.2:p.Ile767Met - ERBB2 p.I767M - ERBB2 p.Ile767Met - HER2 I767M - HER2 I767M Mutation - HER2 Ile767Met - NP_004439.2:p.I767M - NP_004439.2:p.Ile767Met - Proto-Oncogene Neu I767M - Proto-Oncogene Neu Ile767Met - Receptor Tyrosine-Protein Kinase erbB-2 I767M - Receptor Tyrosine-Protein Kinase erbB-2 Ile767Met - Tyrosine Kinase-Type Cell Surface Receptor HER2 I767M - Tyrosine Kinase-Type Cell Surface Receptor HER2 Ile767Met