Canonical Allele Identifier: PA2580423167
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715883
ClinVar RCV Id: RCV002304652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Gln100Arg
CA369953265
NM_018941.4:c.299A>G