Canonical Allele Identifier: PA2580423170
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2042882
ClinVar RCV Id: RCV002908267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ile127Ser
CA369953446
NM_018941.4:c.380T>G