FGFR2c W290G mutant dimer

Stable Identifier
R-HSA-2029930
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participant Of
Disease
Name Identifier Synonyms
Pfeiffer syndrome 14705 acrocephalosyndactylia type V
Crouzon syndrome 2339 Craniofacial Dysostosis