Allele Registry

Canonical Allele Identifier: PA267598

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000087102

RCV000988030

ClinVar Variation:

100736

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Asn264Lys	CA267596 NM_018941.4:c.792C>G CA369954335 NM_018941.4:c.792C>A