Genomics England
GMS Panels
Panels
Genes and Entities
GNB3
G protein subunit beta 3
OMIM:
139130
See this entity in PanelApp
Panel
Mode of inheritance
Details
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1 panel
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in
Retinal disorders
R-numbers:
R32
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Night blindness, congenital stationary, type 1H, OMIM:617024, MONDO:0014872