Varaico: Literature-Extracted Genetic Variants

Gene:SERPINC1
Variant:p.E136_V137Splc
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SERPINC1

NM_000488.4:p.E136_V137Splc

Associated Papers

Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture.

Puurunen M et al.

Journal of Thrombosis and Haemostasis : Jth, 2013

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."