Canonical Allele Identifier: PA2580423179
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2181011
ClinVar RCV Id: RCV002603109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.His202Gln
CA369953941
NM_018941.4:c.606C>A
CA369953942
NM_018941.4:c.606C>G