OPN1LW LOF variants [photoreceptor disc membrane]

Stable Identifier
R-HSA-9918457
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participates
Disease
Name Identifier Synonyms
color blindness DOID:13399 BLINDNESS COLOR, Colour vision deficiency, Colour blindness
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