Canonical Allele Identifier: PA658669702
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 451285
ClinVar RCV Id: RCV000519268 RCV001834700 RCV000550094 RCV001255054 RCV002367739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Leu207Val
CA4599322
NM_018941.4:c.619C>G