Allele Registry

Canonical Allele Identifier: PA102089

Gene: CLN6 HGNC NCBI

ClinVar RCV:

RCV000058915

RCV001787033

ClinVar Variation:

30602

HGVS (amino-acid)	Matching Registered Transcripts
NP_060352.1:p.Arg6Thr	CA259853 NM_017882.3:c.17G>C