Canonical Allele Identifier: PA2573271404
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474193
ClinVar RCV Id: RCV001971081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Asn259Asp
CA170448690
NM_018941.4:c.775A>G