SCN1A c.3071C>G ;(p.A1024G)

Variant ID: 2-166892916-G-C

NM_001165963.1(SCN1A):c.3071C>G;(p.A1024G)

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:

Neurological Disorders and Risk of Arrhythmia.

International Journal Of Molecular Sciences
Bernardi, Joyce J; Aromolaran, Kelly A KA; Aromolaran, Ademuyiwa S AS
Publication Date: 2020-12-27

Variant appearance in text: SCN1A: A1024G
PubMed Link: 33375447
Variant Present in the following documents:
  • Main text
  • ijms-22-00188.pdf
View BVdb publication page