SCN1A c.695G>T ;(p.G232V)

Variant ID: 2-166908498-C-A

NM_001165963.1(SCN1A):c.695G>T;(p.G232V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Application of Trio-Whole Exome Sequencing in Genetic Diagnosis and Therapy in Chinese Children With Epilepsy.

Frontiers In Molecular Neuroscience
Jiang, Tiejia T; Gao, Jia J; Jiang, Lihua L; Xu, Lu L; Zhao, Congying C; Su, Xiaojun X; Shen, Yaping Y; Gu, Weiyue W; Kong, Xiaohong X; Yang, Ying Y; Gao, Feng F
Publication Date: 2021

Variant appearance in text: SCN1A: 695G>T; G232V
PubMed Link: 34489640
Variant Present in the following documents:
  • Main text
  • fnmol-14-699574.pdf
View BVdb publication page