Allele Registry

Canonical Allele Identifier: PA302821

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000175911

RCV000465790

RCV001255074

RCV001704258

RCV002314613

ClinVar Variation:

195348

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Ala4Val	CA302819 NM_018941.4:c.11C>T