Canonical Allele Identifier: PA2573093778
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302488
ClinVar RCV Id: RCV001754377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ile127Met
CA369953447
NM_018941.4:c.381C>G