Canonical Allele Identifier: PA2573271340
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1506915
ClinVar RCV Id: RCV002007076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ser5Arg
CA369952704
NM_018941.4:c.13A>C
CA369952710
NM_018941.4:c.15C>A
CA369952711
NM_018941.4:c.15C>G