Canonical Allele Identifier: PA891856980
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 590039
ClinVar RCV Id: RCV002318223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Phe234Ile
CA369954145
NM_018941.4:c.700T>A