Allele Registry

Canonical Allele Identifier: PA645449906

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000485243

ClinVar Variation:

422177

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Ala155Asp	CA16618619 NM_018941.4:c.464C>A