SCN1A c.1324G>A ;(p.A442T)

Variant ID: 2-166903333-C-T

NM_001165963.1(SCN1A):c.1324G>A;(p.A442T)

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:

Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels.

Pflugers Archiv : European Journal Of Physiology
Baker, Mark D MD; Nassar, Mohammed A MA
Publication Date: 2020-07

Variant appearance in text: SCN1A: A442T
PubMed Link: 32601768
Variant Present in the following documents:
  • Main text
View BVdb publication page