Disorders


 

Paroxysmal Familial Ventricular Fibrillation 1


 

OMIM

GeneLocusProtein
SCN5A3p21Sodium channel protein type 5 subunit alpha

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany  
CGC Genetics - Porto, Portugal  
Health in Code S.L. - A Coruña, Spain  
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

Loading...