Canonical Allele Identifier: PA2829479889
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047618
ClinVar RCV Id: RCV003761198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Leu53Pro
CA363589572
NM_004159.5:c.158T>C