Canonical Allele Identifier: PA2580423694
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161147
ClinVar RCV Id: RCV003087898 RCV003883879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Val261Ala
CA369954313
NM_018941.4:c.782T>C