C98654Level 5
EGFR NP_005219.2:p.D770_N771insN
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** An insertion of the amino acid asparagine between the aspartic acid at position 770 and the asparagine at position 771 of the epidermal growth factor receptor protein.
**Synonyms:** - EGFR D770_N771insN - EGFR N771 Duplication Mutation - EGFR NP_005219.2:p.Asp770_Asn771insAsn - EGFR NP_005219.2:p.N771dup - EGFR p.D770_N771insN - Epidermal Growth Factor Receptor D770_N771insN - NP_005219.2:p.Asn771dup - NP_005219.2:p.Asp770_Asn771insAsn - NP_005219.2:p.D770_N771insN - NP_005219.2:p.N771dup - Proto-Oncogene c-ErbB-1 D770_N771insN - Receptor Tyrosine-Protein Kinase erbB-1 D770_N771insN
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Cross-system equivalences0
No cross-system equivalences mapped for this node.