Allele Registry

Canonical Allele Identifier: PA104200

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000050118

ClinVar Variation:

56705

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Gln76Arg	CA264161 NM_018941.4:c.227A>G