EGFR NP_005219.2:p.V774_C775insHV

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** An insertion of the amino acid sequence histidine-valine between the valine at position 774 and the cysteine at position 775 of the epidermal growth factor receptor protein.

**Synonyms:** - EGFR H773_V774 Duplication Mutation - EGFR NP_005219.2:p.H773_V774dup - EGFR NP_005219.2:p.Val774_Cys775insHisVal - EGFR V774_C775insHV - EGFR p.V774_C775insHV - Epidermal Growth Factor Receptor V774_C775insHV - NP_005219.2:p.H773_V774dup - NP_005219.2:p.His773_Val774dup - NP_005219.2:p.V774_C775insHV - NP_005219.2:p.Val774_Cys775insHisVal - Proto-Oncogene c-ErbB-1 V774_C775insHV - Receptor Tyrosine-Protein Kinase erbB-1 V774_C775insHV