Allele Registry

Canonical Allele Identifier: PA238908

Gene: CLN6 HGNC NCBI

ClinVar Allele:

190553

ClinVar RCV:

RCV000187111

RCV000515438

RCV000766779

RCV001085594

RCV002313023

RCV003917602

ClinVar Variation:

193389

HGVS (amino-acid)	Matching Registered Transcripts
NP_060352.1:p.Ala18Val	CA238907 NM_017882.3:c.53C>T