Canonical Allele Identifier: PA302821
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 195348
ClinVar RCV Id: RCV000175911 RCV000465790 RCV001704258 RCV002314613 RCV001255074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ala4Val
CA302819
NM_018941.4:c.11C>T