Canonical Allele Identifier: PA2573271380
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1679851
ClinVar RCV Id: RCV002227867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.His139Arg
CA369953520
NM_018941.4:c.416A>G