Canonical Allele Identifier: PA658819201
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 499266
ClinVar RCV Id: RCV000596520 RCV002531040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ala51Thr
CA4599214
NM_018941.4:c.151G>A