Canonical Allele Identifier: PA2573271372
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431099
ClinVar RCV Id: RCV001952625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ala120Ser
CA369953403
NM_018941.4:c.358G>T