Allele Registry

Canonical Allele Identifier: PA645445969

Gene: ARL13B HGNC NCBI

ClinVar Variation Id: 346913

HGVS (amino-acid)	Matching Registered Transcripts
NP_878899.1:p.Gly384Glu	CA2504290 NM_182896.3:c.1151G>A