TTN c.4762G>T ;(p.V1588L)

Variant ID: 2-179641928-C-A

NM_001267550.1(TTN):c.4762G>T;(p.V1588L)

This variant was identified in 1 publication

View GRCh38 version.




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: V1588L
PubMed Link: 28323875
Variant Present in the following documents:
  • Main text
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