Allele Registry

Canonical Allele Identifier: PA109512

Gene: ARL13B HGNC NCBI

ClinVar RCV:

RCV000002068

ClinVar Variation:

1991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167621.1:p.Arg79Gln	CA252019 NM_001174150.2:c.236G>A