Canonical Allele Identifier: PA104299
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56710
ClinVar RCV Id: RCV000050123 RCV001377678 RCV002483067 RCV002514269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Tyr158Cys
CA264172
NM_018941.4:c.473A>G