Allele Registry

Canonical Allele Identifier: PA2827105879

Gene: ARL13B HGNC NCBI

ClinVar RCV:

RCV000002068

ClinVar Variation:

1991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308257.1:p.Arg64Gln	CA252019 NM_001321328.2:c.191G>A