Activated FGFR2c W290G mutant

Stable Identifier
R-HSA-2029913
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