Allele Registry

Canonical Allele Identifier: PA264187

Gene: CLN8 HGNC NCBI

ClinVar RCV:

RCV000050129

ClinVar Variation:

56716

HGVS (amino-acid)	Matching Registered Transcripts
NP_061764.2:p.Trp213del	CA264185 NM_018941.4:c.637_639del