Canonical Allele Identifier: PA2580423171
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2039600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Cys149Tyr
CA369953584
NM_018941.4:c.446G>A