EGFR NM_005228.3:c.787A>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 787 of the coding sequence of the EGFR gene where adenine has been mutated to cytosine.

**Synonyms:** - EGFR c.787A>C - ERBB c.787A>C - ERBB1 c.787A>C - Epidermal Growth Factor Receptor Gene c.787A>C - HER1 c.787A>C - NM_005228.3:c.787A>C