SCN1A c.1726A>G ;(p.S576G)

Variant ID: 2-166900496-T-C

NM_001165963.1(SCN1A):c.1726A>G;(p.S576G)

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:

Genetic Diagnosis in Children with Epilepsy and Developmental Disorders by Targeted Gene Panel Analysis in a Developing Country.

Journal Of Epilepsy Research
Rahman, Md Mizanur MM; Fatema, Kanij K
Publication Date: 2021-06

Variant appearance in text: SCN1A: 1726A>G; Ser576Gly
PubMed Link: 34395220
Variant Present in the following documents:
  • jer-21004.pdf
View BVdb publication page