Allele Registry

Canonical Allele Identifier: PA264169

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000050121

ClinVar Variation:

56708

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Ala155Val	CA264167 NM_018941.4:c.464C>T