Canonical Allele Identifier: PA2499285249
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014772
ClinVar RCV Id: RCV001313553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ser12Thr
CA369952749
NM_018941.4:c.35G>C