WNK4 c.1184A>C ;(p.N395T)

Variant ID: 17-40937128-A-C

NM_032387.4(WNK4):c.1184A>C;(p.N395T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting.

Journal Of Medical Genetics
Bao, Minghui M; Li, Ping P; Li, Qifu Q; Chen, Hui H; Zhong, Ying Y; Li, Shuangyue S; Jin, Ling L; Wang, Wenjie W; Chen, Zhenzhen Z; Zhong, Jiuchang J; Geng, Bin B; Fan, Yuxin Y; Yang, Xinchun X; Cai, Jun J
Publication Date: 2020-08

Variant appearance in text: WNK4: N395T
PubMed Link: 32561571
Variant Present in the following documents:
  • jmedgenet-2019-106145supp001.pdf
View BVdb publication page