SCN1A c.1746G>A ;(p.K582=)

Variant ID: 2-166900476-C-T

NM_001165963.1(SCN1A):c.1746G>A;(p.K582=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.

Human Genomics
Domitrz, Izabela I; Kosiorek, Michalina M; Żekanowski, Cezary C; Kamińska, Anna A
Publication Date: 2016-01-08

Variant appearance in text: SCN1A: 1746G>A
PubMed Link: 26747084
Variant Present in the following documents:
  • Main text
  • 40246_2015_Article_57.pdf
View BVdb publication page