Allele Registry

Canonical Allele Identifier: PA104220

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000050130

RCV000711267

RCV001221743

RCV001804787

ClinVar Variation:

56717

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Gly221Ser	CA264188 NM_018941.4:c.661G>A