SCN5A c.1018C>G ;(p.R340G)

Variant ID: 3-38648282-G-C

NM_000335.4(SCN5A):c.1018C>G;(p.R340G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Atrial fibrillation: the role of common and rare genetic variants.

European Journal Of Human Genetics : Ejhg
Olesen, Morten S MS; Nielsen, Morten W MW; Haunsø, Stig S; Svendsen, Jesper H JH
Publication Date: 2014-03

Variant appearance in text: SCN5A: 1018C>G
PubMed Link: 23838598
Variant Present in the following documents:
  • Main text
View BVdb publication page