Canonical Allele Identifier: PA2580423180
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1898153
ClinVar RCV Id: RCV002579773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Met205Val
CA369953955
NM_018941.4:c.613A>G