EGFR NP_005219.2:p.D770_N771insNPH
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** An insertion of the amino acid sequence asparagine-proline-histidine between the aspartic acid at position 770 and the asparagine at position 771 of the epidermal growth factor receptor protein.
**Synonyms:** - EGFR D770_N771insNPH - EGFR N771_H773 Duplication Mutation - EGFR NP_005219.2:p.Asp770_Asn771insAsnProHis - EGFR NP_005219.2:p.N771_H773dup - EGFR p.D770_N771insNPH - Epidermal Growth Factor Receptor D770_N771insNPH - NP_005219.2:p.Asn771_His773dup - NP_005219.2:p.Asp770_Asn771insAsnProHis - NP_005219.2:p.D770_N771insNPH - NP_005219.2:p.N771_H773dup - Proto-Oncogene c-ErbB-1 D770_N771insNPH - Receptor Tyrosine-Protein Kinase erbB-1 D770_N771insNPH
/api/v1/systems/nci_thesaurus/nodes/C98656Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.