Canonical Allele Identifier: PA2580423172
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2146768
ClinVar RCV Id: RCV003076846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Leu153Val
CA369953607
NM_018941.4:c.457C>G