Canonical Allele Identifier: PA2573271378
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Phe131Cys
CA369953470
NM_018941.4:c.392T>G