Canonical Allele Identifier: PA1139729546
Gene: CLN8 HGNC NCBI

Linked Data

ClinVar Variation Id: 842621
ClinVar RCV Id: RCV001045066 RCV001832430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061764.2:p.Ile137Met
CA4599261
NM_018941.4:c.411C>G