SCN5A c.2466G>C ;(p.W822C)

Variant ID: 3-38627503-C-G

NM_000335.4(SCN5A):c.2466G>C;(p.W822C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.

Journal Of The American College Of Cardiology
Crotti, Lia L; Marcou, Cherisse A CA; Tester, David J DJ; Castelletti, Silvia S; Giudicessi, John R JR; Torchio, Margherita M; Medeiros-Domingo, Argelia A; Simone, Savastano S; Will, Melissa L ML; Dagradi, Federica F; Schwartz, Peter J PJ; Ackerman, Michael J MJ
Publication Date: 2012-10-09

Variant appearance in text: SCN5A: W822C
PubMed Link: 22840528
Variant Present in the following documents:
  • Main text
View BVdb publication page