Allele Registry

Canonical Allele Identifier: PA102047

Gene: CLN6 HGNC NCBI

ClinVar RCV:

RCV000551912

ClinVar Variation:

457972

HGVS (amino-acid)	Matching Registered Transcripts
NP_060352.1:p.Arg149Cys	CA7630608 NM_017882.3:c.445C>T