Prothrombin gene mutation (or Factor II mutation or Prothrombin G20210A) is an inherited condition that increases your predisposition to develop abnormal blood clots in the veins (deep vein thrombosis or DVT) and lungs (pulmonary embolism or PE).
Sample Type - Blood
Reporting Time - 4 Days
Prerequisites - No special preparation required
Price - ₹4000/-
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