Allele Registry

Canonical Allele Identifier: PA264158

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000050116

ClinVar Variation:

56703

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Lys61del	CA264156 NM_018941.4:c.181_183del