SCN5A c.4285G>A ;(p.D1429N)

Variant ID: 3-38598733-C-T

NM_000335.4(SCN5A):c.4285G>A;(p.D1429N)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel SCN5A p.V1429M Variant Segregation in a Family with Brugada Syndrome.

International Journal Of Molecular Sciences
Monasky, Michelle M MM; Micaglio, Emanuele E; Ciconte, Giuseppe G; Borrelli, Valeria V; Giannelli, Luigi L; Vicedomini, Gabriele G; Ghiroldi, Andrea A; Anastasia, Luigi L; Locati, Emanuela T ET; Benedetti, Sara S; Di Resta, Chiara C; Casari, Giorgio G; Pappone, Carlo C
Publication Date: 2020-08-17

Variant appearance in text: SCN5A: 4285G>A; Val1429Met
PubMed Link: 32824506
Variant Present in the following documents:
  • Main text
  • ijms-21-05902.pdf
View BVdb publication page