Allele Registry

Canonical Allele Identifier: PA263699

Gene: CLN3 HGNC NCBI

ClinVar RCV:

RCV000049689

ClinVar Variation:

56277

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035897.1:p.Leu170Pro	CA263696 NM_001042432.2:c.509T>C