Canonical Allele Identifier: PA2829479946
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1693911
ClinVar RCV Id: RCV002261780 RCV003095900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Arg87Trp
CA3746452
NM_004159.5:c.259C>T