Allele Registry

Canonical Allele Identifier: PA2580423173

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV003062152

ClinVar Variation:

2136636

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Thr170Arg	CA369953713 NM_018941.4:c.509C>G