Genomics England
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Genes and Entities
RNF213
ring finger protein 213
OMIM:
613768
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Panel
Mode of inheritance
Details
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in
Cerebral vascular malformations
R-numbers:
R336
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
{Moyamoya disease 2, susceptibility to}, OMIM:607151