FGFR2c A315S mutant dimer [plasma membrane]

Stable Identifier
R-HSA-2071933
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participates
Disease
Name Identifier Synonyms
bone development disease DOID:0080006
syndactyly DOID:11193 Symphalangism, Symphalangy (disorder), (Polysyndactyly) or (symphalangism) or (syndactyly NOS), Webbing of digits
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