Canonical Allele Identifier: PA2573271367
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477553
ClinVar RCV Id: RCV002018768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ala93Gly
CA369953227
NM_018941.4:c.278C>G