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prothrombin genotyping

Clinical significance: - F2 gene p.G20210A mutation associated with hypercoagulability Specimen: - whole blood

Related

prothrombin; coagulation factor II; contains: activation peptide fragment 1; activation peptide fragment 2; thrombin light chain; thrombin heavy chain (F2)

Specific

prothrombin (F2) gene p.G20210A

General

genotyping (allele testing)

References

  1. Primerdesign: Prothrombin genotyping kit http://highresolutionmelt.co.uk/Download%20material/Prothrombin%20Handbook.pdf