Allele Registry

Canonical Allele Identifier: PA263628

Gene: CLN3 HGNC NCBI

ClinVar RCV:

RCV000049664

RCV003317069

ClinVar Variation:

56252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035897.1:p.Asp416Gly	CA263624 NM_001042432.2:c.1247A>G