Allele Registry

Canonical Allele Identifier: PA645449753

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000433355

ClinVar Variation:

392756

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Ala30Thr	CA4599195 NM_018941.4:c.88G>A