SCN5A c.393G>C ;(p.S131=)

Variant ID: 3-38663980-C-G

NM_000335.4(SCN5A):c.393G>C;(p.S131=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies.

Cardiovascular Therapeutics
Amarouch, Mohamed-Yassine MY; El Hilaly, Jaouad J
Publication Date: 2020

Variant appearance in text: PFHB1: 393G>C
PubMed Link: 33381229
Variant Present in the following documents:
  • Main text
View BVdb publication page