Canonical Allele Identifier: PA100381
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 659832
ClinVar RCV Id: RCV000663373 RCV000816894 RCV003411802 RCV003596608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Thr75Met
CA3746458
NM_148919.4:c.224C>T