Canonical Allele Identifier: PA104231
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 188917
ClinVar RCV Id: RCV000169279 RCV000187126 RCV003532006
ClinVar Variation Id: 2100686
ClinVar RCV Id: RCV003014527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Gly237Arg
CA274121
NM_018941.4:c.709G>A
CA369954161
NM_018941.4:c.709G>C