SCN1A c.2213G>A ;(p.W738*)

Variant ID: 2-166897943-C-T

NM_001165963.1(SCN1A):c.2213G>A;(p.W738*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Epilepsy-Related Voltage-Gated Sodium Channelopathies: A Review.

Frontiers In Pharmacology
Menezes, Luis Felipe Santos LFS; Sabiá Júnior, Elias Ferreira EF; Tibery, Diogo Vieira DV; Carneiro, Lilian Dos Anjos LDA; Schwartz, Elisabeth Ferroni EF
Publication Date: 2020

Variant appearance in text: SCN1A: W738X
PubMed Link: 33013363
Variant Present in the following documents:
  • Main text
View BVdb publication page