Canonical Allele Identifier: PA104249
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56706
ClinVar RCV Id: RCV000050119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ile107Ser
CA264163
NM_018941.4:c.320T>G