Canonical Allele Identifier: PA658819196
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 521986
ClinVar RCV Id: RCV000623561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Gly31Asp
CA369952852
NM_018941.4:c.92G>A