Canonical Allele Identifier: PA2829480000
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_004150.1:p.Leu127Pro
CA363589090
NM_004159.5:c.380T>C