Canonical Allele Identifier: PA2829479887
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 356367
ClinVar RCV Id: RCV000266887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Ser52Tyr
CA10626482
NM_004159.5:c.155C>A