SCN5A c.5723A>G ;(p.Q1908R)

Variant ID: 3-38592137-T-C

NM_000335.4(SCN5A):c.5723A>G;(p.Q1908R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype.

Pharmacogenomics And Personalized Medicine
Fonseca, Dora Janeth DJ; Morel, Adrien A; Llinás-Caballero, Kevin K; Bolívar-Salazar, David D; Laissue, Paul P
Publication Date: 2021

Variant appearance in text: SCN5A: 5723A>G
PubMed Link: 33688237
Variant Present in the following documents:
  • Main text
View BVdb publication page