rs376923877

This is a variant in the TNNT2 gene that changes a asparagine to an lysine.

ClinVar annotation

Pathogenic☆☆☆
2 submitters6 publications

Cardiovascular phenotype; Hypertrophic cardiomyopathy

View on ClinVar →

About TNNT2

This gene encodes the cardiac isoform of troponin T. The encoded protein is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy. [provided by RefSeq, May 2022]

View all TNNT2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…