EGFR NM_005228.3:c.2153T>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 2153 of the coding sequence of the EGFR gene where thymine has been mutated to adenine.

**Synonyms:** - EGFR c.2153T>A - ERBB c.2153T>A - ERBB1 c.2153T>A - Epidermal Growth Factor Receptor Gene c.2153T>A - HER1 c.2153T>A - NM_005228.3:c.2153T>A