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81414 - Genetic Testing Cardiac ion channelopathies (eg, Brugada syndrome, long QT

This procedure appears on the selected insurer prior authorization source.

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Procedure / ServiceGenetic Testing Cardiac ion channelopathies (eg, Brugada syndrome, long QT
Procedure / Service Description

Canavan disease, cystic fibrosis, familial dysautonomia, Fanconi - including ANK2, CASQ2, CAV3, KCN Genetic Testing 81414 Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholaminergic polymorphic

Likely documents
  • Confirm benefit details
  • Submit clinical notes if requested by the plan
Next actions
  • Confirm the current plan policy before submission.
  • Use the insurer authorization workflow for this listed code.