Allele Registry

Canonical Allele Identifier: PA104249

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000050119

ClinVar Variation:

56706

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Ile107Ser	CA264163 NM_018941.4:c.320T>G