SCN1A c.890C>A ;(p.T297N)

Variant ID: 2-166908303-G-T

NM_001165963.1(SCN1A):c.890C>A;(p.T297N)

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:

Do All Roads Lead to Rome? Genes Causing Dravet Syndrome and Dravet Syndrome-Like Phenotypes.

Frontiers In Neurology
Ding, Jiangwei J; Wang, Lei L; Jin, Zhe Z; Qiang, Yuanyuan Y; Li, Wenchao W; Wang, Yangyang Y; Zhu, Changliang C; Jiang, Shucai S; Xiao, Lifei L; Hao, Xiaoyan X; Hu, Xulei X; Li, Xinxiao X; Wang, Feng F; Sun, Tao T
Publication Date: 2022

Variant appearance in text: SCN1A: 890C>A
PubMed Link: 35359639
Variant Present in the following documents:
  • Main text
  • fneur-13-832380.pdf
View BVdb publication page