TTN c.26080G>A ;(p.E8694K)

Variant ID: 2-179579833-C-T

NM_001267550.1(TTN):c.26080G>A;(p.E8694K)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

The clinical features, outcomes and genetic characteristics of hypertrophic cardiomyopathy patients with severe right ventricular hypertrophy.

Plos One
Guo, Xiying X; Fan, Chaomei C; Tian, Lei L; Liu, Yanling Y; Wang, Hongyue H; Zhao, Shihua S; Duan, Fujian F; Zhang, Xiuling X; Zhao, Xing X; Wang, Fengqi F; Zhu, Hongguang H; Lin, Aiqing A; Wu, Xia X; Li, Yishi Y
Publication Date: 2017

Variant appearance in text: TTN: E8694K
PubMed Link: 28323875
Variant Present in the following documents:
  • Main text
  • pone.0174118.pdf
View BVdb publication page