Canonical Allele Identifier: PA104200
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56705
ClinVar RCV Id: RCV000050118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Gln76Arg
CA264161
NM_018941.4:c.227A>G