Allele Registry

Canonical Allele Identifier: PA252024

Gene: ARL13B HGNC NCBI

ClinVar RCV:

RCV000002070

RCV003330381

ClinVar Variation:

1993

HGVS (amino-acid)	Matching Registered Transcripts
NP_878899.1:p.Arg200Cys	CA252023 NM_182896.3:c.598C>T