Canonical Allele Identifier: PA645400085
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_683720.2:p.Ser56Tyr
CA10626482
NM_148919.4:c.167C>A