TTN c.66498dup ;(p.D22167*)

Variant ID: 2-179446496-C-CA

NM_001267550.1(TTN):c.66498dup;(p.D22167*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndrome.

Heart Rhythm O2
Giudicessi, John R JR; Maleszewski, Joseph J JJ; Tester, David J DJ; Ackerman, Michael J MJ
Publication Date: 2021-10

Variant appearance in text: N/A
PubMed Link: 34667957
Variant Present in the following documents:
View BVdb publication page