TTN c.76849_76850insGC ;(p.S25617Cfs*18)

Variant ID: 2-179434009-G-GGC

NM_001267550.1(TTN):c.76849_76850insGC;(p.S25617Cfs*18)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.

European Heart Journal
Akinrinade, Oyediran O; Ollila, Laura L; Vattulainen, Sanna S; Tallila, Jonna J; Gentile, Massimiliano M; Salmenperä, Pertteli P; Koillinen, Hannele H; Kaartinen, Maija M; Nieminen, Markku S MS; Myllykangas, Samuel S; Alastalo, Tero-Pekka TP; Koskenvuo, Juha W JW; Heliö, Tiina T
Publication Date: 2015-09-07

Variant appearance in text: TTN: Ser25617Cysfs*18
PubMed Link: 26084686
Variant Present in the following documents:
  • Main text
  • ehv253.pdf
View BVdb publication page