Canonical Allele Identifier: PA104152
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Arg204Cys
CA252418
NM_018941.4:c.610C>T