TNNT2 c.68-8A>G

Variant ID: 1-201338981-T-C

NM_001276345.1(TNNT2):c.68-8A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.

Cardiovascular Journal Of Africa
Ntusi, Ntobeko A NA; Shaboodien, Gasnat G; Badri, Motasim M; Gumedze, Freedom F; Mayosi, Bongani M BM
Publication Date: 2016

Variant appearance in text: rs115805892
PubMed Link: 27841901
Variant Present in the following documents:
  • Main text
  • cvja-27-152.pdf
View BVdb publication page