Varaico: Literature-Extracted Genetic Variants

Gene:FGG
Variant:p.D390Y
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FGG

NM_021870.3:p.D390Y

Associated Papers

A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype.

Xu N et al.

Hereditas, 2024

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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."