Allele Registry

Canonical Allele Identifier: PA2826112205

Gene: ARL13B HGNC NCBI

ClinVar RCV:

RCV000256476

RCV001092355

RCV001859504

ClinVar Variation:

266096

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167621.1:p.Arg200His	CA2504099 NM_001174150.2:c.599G>A