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GTR Home > Tests > Cardiac channelopathy Comprehensive panel


Test order codeHelp: 5320

Test name


Cardiac channelopathy Comprehensive panel

Purpose of the test


This is a clinical test intended for Help: Diagnosis, Mutation Confirmation



Click Indication tab for more information.

How to order


Please use the equisition form and easy-to-use submission instructions available on the CTGT web site
Order URL Help: http://ctgt.net/how-to-order

Specimen source

Cell culture
Cord blood
Isolated DNA
Peripheral (whole) blood
White blood cell prep
Specimen requirements: http://www.ctgt.net/order/specimens


Molecular Genetics
DDeletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
TTargeted variant analysis
Bi-directional Sanger Sequence Analysis

Summary of what is tested

Click Methodology tab for more information.

Clinical utility


Not provided

Clinical validity


Not provided

Test services

  • Clinical Testing/Confirmation of Mutations Identified Previously, Order code: 5320
  • Confirmation of research findings
  • Custom Prenatal Testing, comments
  • Custom mutation-specific/Carrier testing

Clinical resources

Practice guidelines

  • HRS/EHRA, 2012
    HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.