Canonical Allele Identifier: PA104181
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 205207
ClinVar RCV Id: RCV000187142 RCV000677331 RCV000656837 RCV001080578 RCV001251946 RCV002314707 RCV003224205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Asn125Ser
CA314053
NM_018941.4:c.374A>G