Allele Registry

Canonical Allele Identifier: PA2830262572

Gene: ARL13B HGNC NCBI

ClinVar RCV:

RCV000726050

RCV001082926

RCV003940043

ClinVar Variation:

287670

HGVS (amino-acid)	Matching Registered Transcripts
NP_659433.2:p.Asn170Lys	CA2504195 NM_144996.4:c.510C>A CA353678872 NM_144996.4:c.510C>G