EGFR NM_005228.3:c.866C>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 866 of the coding sequence of the EGFR gene where cytosine has been mutated to adenine.

**Synonyms:** - EGFR c.866C>A - ERBB c.866C>A - ERBB1 c.866C>A - Epidermal Growth Factor Receptor Gene c.866C>A - HER1 c.866C>A - NM_005228.3:c.866C>A