Canonical Allele Identifier: PA2580516298
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1694138
ClinVar RCV Id: RCV002262007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Leu131Pro
CA363589090
NM_148919.4:c.392T>C