SCN4B c.438C>A ;(p.T146=)

Variant ID: 11-118014573-G-T

NM_174934.3(SCN4B):c.438C>A;(p.T146=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy.

Applied & Translational Genomics
Refsgaard, Lena L; Olesen, Morten Salling MS; Møller, Daniel Vega DV; Christiansen, Michael M; Haunsø, Stig S; Svendsen, Jesper Hastrup JH; Christensen, Alex Hørby AH
Publication Date: 2012-12-01

Variant appearance in text: SCN4B: T146T
PubMed Link: 27896052
Variant Present in the following documents:
  • main.pdf
View BVdb publication page