EGFR NM_005228.3:c.1476C>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1476 of the coding sequence of the EGFR gene where cytosine has been mutated to adenine.

**Synonyms:** - EGFR S492R Gene Mutation - EGFR c.1476C>A - ERBB c.1476C>A - ERBB1 c.1476C>A - Epidermal Growth Factor Receptor Gene c.1476C>A - HER1 c.1476C>A - NM_005228.3:c.1476C>A