F8 light chain thrombin cleavage site variants [extracellular region]

Stable Identifier
R-HSA-9666399
Type
Complex
Species
Homo sapiens
Compartment
extracellular region
Synonyms
FVIII light chain thrombin cleavage site variants
Locations in the PathwayBrowser
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Participants
components
Participates
as a member of
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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