Canonical Allele Identifier: PA1139729680
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 946754
ClinVar RCV Id: RCV001217680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Val206Phe
CA369953963
NM_018941.4:c.616G>T