Allele Registry

Canonical Allele Identifier: PA252020

Gene: ARL13B HGNC NCBI

ClinVar RCV:

RCV000002068

ClinVar Variation:

1991

HGVS (amino-acid)	Matching Registered Transcripts
NP_878899.1:p.Arg79Gln	CA252019 NM_182896.3:c.236G>A