Canonical Allele Identifier: PA1139729532
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 991259
ClinVar RCV Id: RCV001279443 RCV001363688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ser124Tyr
CA369953428
NM_018941.4:c.371C>A