Allele Registry

Canonical Allele Identifier: PA2830262694

Gene: ARL13B HGNC NCBI

ClinVar Variation Id: 346913

HGVS (amino-acid)	Matching Registered Transcripts
NP_659433.2:p.Gly277Glu	CA2504290 NM_144996.4:c.830G>A