Varaico: Literature-Extracted Genetic Variants

Gene:F2
Variant:p.H605fs
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F2

NM_000506.5:p.H605fs

Associated Papers

A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene.

Mansory EM et al.

Research and Practice in Thrombosis and Haemostasis, 2021

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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."