ClinVar Miner

Submissions for variant NM_000129.4(F13A1):c.1860_1861delinsCT (p.Ala621Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV003313878 SCV004013080 uncertain significance Thrombophilia due to thrombin defect criteria provided, single submitter clinical testing

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