SCN5A c.5111T>C ;(p.F1704S)

Variant ID: 3-38592749-A-G

NM_000335.4(SCN5A):c.5111T>C;(p.F1704S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


SCN5A Variants: Association With Cardiac Disorders.

Frontiers In Physiology
Li, Wenjia W; Yin, Lei L; Shen, Cheng C; Hu, Kai K; Ge, Junbo J; Sun, Aijun A
Publication Date: 2018

Variant appearance in text: LQT3: 5111T>C
PubMed Link: 30364184
Variant Present in the following documents:
  • Main text
  • fphys-09-01372.pdf
View BVdb publication page