Allele Registry

Canonical Allele Identifier: PA279442

Gene: ARL13B HGNC NCBI

ClinVar Allele:

214168

ClinVar RCV:

RCV000201642

ClinVar Variation:

217551

HGVS (amino-acid)	Matching Registered Transcripts
NP_878899.1:p.Val22Gly	CA279441 NM_182896.3:c.65T>G