Canonical Allele Identifier: PA2829479911
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2147267
ClinVar RCV Id: RCV003596192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.His67Arg
CA363589483
NM_004159.5:c.200A>G