C189905Level 6
Non-synonymous ERBB2 Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation in the ERBB2 gene that encodes an amino acid substitution in the receptor tyrosine-protein kinase erbB-2 protein.
**Synonyms:** - ERBB2 Missense Mutation - Non-synonymous Erb-B2 Receptor Tyrosine Kinase 2 Gene Mutation - Non-synonymous HER2 Gene Mutation - Non-synonymous HER2/neu Gene Mutation - Non-synonymous NEU Gene Mutation - Non-synonymous v-Erb-B2 Avian Erythroblastic Leukemia Viral Oncogene Homolog 2 Gene Mutation
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