ERBB2 NM_004448.4:c.2632C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 2632 of the coding sequence of the ERBB2 gene where cytosine has been mutated to thymine.

**Synonyms:** - ERBB2 c.2632C>T - Erb-b2 Receptor Tyrosine Kinase 2 c.2632C>T - HER-2 c.2632C>T - HER-2/neu c.2632C>T - HER2 c.2632C>T - NEU c.2632C>T - NM_004448.4:c.2632C>T