Canonical Allele Identifier: PA1139750195
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 835890
ClinVar RCV Id: RCV001036886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Arg129His
CA3746401
NM_148919.4:c.386G>A