Canonical Allele Identifier: PA104159
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2802
ClinVar RCV Id: RCV000002936 RCV000409951 RCV000820654 RCV004525841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Arg24Gly
CA340024
NM_018941.4:c.70C>G