Canonical Allele Identifier: PA2830290086
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3220392
ClinVar RCV Id: RCV004513302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Cys120Arg
CA3746406
NM_148919.4:c.358T>C