SCN5A c.2162T>C ;(p.L721P)

Variant ID: 3-38639320-A-G

NM_000335.4(SCN5A):c.2162T>C;(p.L721P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Etiology of sudden death in the community: results of anatomical, metabolic, and genetic evaluation.

American Heart Journal
Adabag, A Selcuk AS; Peterson, Garry G; Apple, Fred S FS; Titus, Jack J; King, Richard R; Luepker, Russell V RV
Publication Date: 2010-01

Variant appearance in text: SCN5A: L721P
PubMed Link: 20102864
Variant Present in the following documents:
  • Main text
View BVdb publication page