Canonical Allele Identifier: PA2573271387
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512278
ClinVar RCV Id: RCV002045620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Trp195Arg
CA4599316
NM_018941.4:c.583T>C
CA369953884
NM_018941.4:c.583T>A