Canonical Allele Identifier: PA645449957
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 424331
ClinVar RCV Id: RCV000479521 RCV001273356 RCV001851272 RCV003278837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ala266Thr
CA4599354
NM_018941.4:c.796G>A