Canonical Allele Identifier: PA314063
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 205210
ClinVar RCV Id: RCV000187145 RCV000706746 RCV001833114 RCV002513993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Asn259Ser
CA314061
NM_018941.4:c.776A>G