Allele Registry

Canonical Allele Identifier: PA645449750

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000478754

RCV001835821

ClinVar Variation:

423135

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Ala30Ser	CA4599194 NM_018941.4:c.88G>T