Canonical Allele Identifier: PA2580423154
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2103550
ClinVar RCV Id: RCV003022207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Asn2Ser
CA369952691
NM_018941.4:c.5A>G