Canonical Allele Identifier: PA104171
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56704
ClinVar RCV Id: RCV000050117 RCV000464589 RCV000623329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Arg70His
CA264159
NM_018941.4:c.209G>A