Allele Registry

Canonical Allele Identifier: PA658819201

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000596520

RCV002531040

ClinVar Variation:

499266

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Ala51Thr	CA4599214 NM_018941.4:c.151G>A