Activated FGFR2 N549H mutant [plasma membrane]

Stable Identifier
R-HSA-2033315
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participates
Disease
Name Identifier Synonyms
Crouzon syndrome DOID:2339 Craniofacial Dysostosis
bone development disease DOID:0080006
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