TTN c.26656G>C ;(p.G8886R)

Variant ID: 2-179578729-C-G

NM_001267550.1(TTN):c.26656G>C;(p.G8886R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Role of Titin Missense Variants in Dilated Cardiomyopathy.

Journal Of The American Heart Association
Begay, Rene L RL; Graw, Sharon S; Sinagra, Gianfranco G; Merlo, Marco M; Slavov, Dobromir D; Gowan, Katherine K; Jones, Kenneth L KL; Barbati, Giulia G; Spezzacatene, Anita A; Brun, Francesca F; Di Lenarda, Andrea A; Smith, John E JE; Granzier, Henk L HL; Mestroni, Luisa L; Taylor, Matthew M; ,
Publication Date: 2015-11-13

Variant appearance in text: TTN: 26656G>C; Gly8886Arg
PubMed Link: 26567375
Variant Present in the following documents:
  • Main text
  • JAH3-4-e002645.pdf
View BVdb publication page