BTK NM_000061.3:c.1441T>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1141 of the coding sequence of the BTK gene where thymine has been mutated to adenine.

**Synonyms:** - ATK c.1441T>A - BPK c.1441T>A - BTK c.1441T>A - Bruton Agammaglobulinemia Tyrosine Kinase c.1441T>A - Bruton Tyrosine Kinase c.1441T>A - NM_000061.3:c.1441T>A - PSCTK1 c.1441T>A