EGFR NP_005219.2:p.Y764_V765insHH

MedGen UID:: 475920
•Concept ID:: C3274287
•: Cell or Molecular Dysfunction

Synonyms:

EGFR NP_005219.2:p.Tyr764_Val765insHisHis; EGFR p.Y764_V765insHH; EGFR Y764_V765insHH; Epidermal Growth Factor Receptor Y764_V765insHH; NP_005219.2:p.Y764_V765insHH; Proto-Oncogene c-ErbB-1 Y764_V765insHH; Receptor Tyrosine-Protein Kinase erbB-1 Y764_V765insHH

Definition

An insertion of the amino acid sequence histidine-histidine between the tyrosine at position 764 and the valine at position 765 of the epidermal growth factor receptor protein. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVEGFR NP_005219.2:p.Y764_V765insHH

Molecular Abnormality
- Molecular Sequence Variation
  - Gene Product Sequence Variation
    - EGFR Protein Variant
      - EGFR NP_005219.2:p.Y764_V765insHH

Supplemental Content

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