EGFR NM_005228.3:c.2369C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 2369 of the coding sequence of the EGFR gene where cytosine has been mutated to thymine.

**Synonyms:** - EGFR c.2369C>T - ERBB c.2369C>T - ERBB1 c.2369C>T - Epidermal Growth Factor Receptor Gene c.2369C>T - HER1 c.2369C>T - NM_005228.3:c.2369C>T