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