Allele Registry

Canonical Allele Identifier: PA2827105914

Gene: ARL13B HGNC NCBI

ClinVar Allele:

214169

ClinVar RCV:

RCV000201595

RCV002282036

ClinVar Variation:

217552

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308257.1:p.Asn139Ser	CA277722 NM_001321328.2:c.416A>G