EGFR NP_005219.2:p.H773_V774insH

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** An insertion of the amino acid histidine between the histidine at position 773 and the valine at position 774 of the epidermal growth factor receptor protein.

**Synonyms:** - EGFR H773 Duplication Mutation - EGFR H773_V774insH - EGFR NP_005219.2:p.H773dup - EGFR NP_005219.2:p.His773_Val774insHis - EGFR p.H773_V774insH - Epidermal Growth Factor Receptor H773_V774insH - NP_005219.2:p.H773_V774insH - NP_005219.2:p.H773dup - NP_005219.2:p.His773_Val774insHis - NP_005219.2:p.His773dup - Proto-Oncogene c-ErbB-1 H773_V774insH - Receptor Tyrosine-Protein Kinase erbB-1 H773_V774insH