Canonical Allele Identifier: PA2573271395
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1348111
ClinVar RCV Id: RCV002044152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Tyr227Phe
CA4599334
NM_018941.4:c.680A>T