Canonical Allele Identifier: PA2741971160
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2693725
ClinVar RCV Id: RCV003533886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Thr26Ser
CA369952825
NM_018941.4:c.76A>T