SCN1A c.5389G>T ;(p.A1797S)

Variant ID: 2-166848396-C-A

NM_001165963.1(SCN1A):c.5389G>T;(p.A1797S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases.

Frontiers In Molecular Neuroscience
Chen, Chunhong C; Fang, Fang F; Wang, Xu X; Lv, Junlan J; Wang, Xiaohui X; Jin, Hong H
Publication Date: 2022

Variant appearance in text: SMEI: 5389G>T
PubMed Link: 35571373
Variant Present in the following documents:
  • Main text
  • fnmol-15-821012.pdf
View BVdb publication page