Canonical Allele Identifier: PA2741971166
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2688795
ClinVar RCV Id: RCV003490574 RCV004364875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Phe201Ile
CA369953927
NM_018941.4:c.601T>A