Canonical Allele Identifier: PA2829479931
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 583398
ClinVar RCV Id: RCV000707724 RCV002261198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Ala73Thr
CA3746457
NM_004159.5:c.217G>A