Canonical Allele Identifier: PA645400087
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 356363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Arg229His
CA3746314
NM_148919.4:c.686G>A