Bibliome.ai browser hg19
Search
About
Stats
FAQ
SCN1A c.5641G>T ;(p.E1881*)
Variant ID: 2-166848144-C-A
NM_001165963.1(
SCN1A
):c.5641G>T;(p.E1881*)
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:
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: E1881X
PubMed Link:
33013363
Variant Present in the following documents:
Main text
fphar-11-01276.pdf
View BVdb publication page