Canonical Allele Identifier: PA1139750191
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 870500
ClinVar RCV Id: RCV001093597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Asp123Asn
CA363589149
NM_148919.4:c.367G>A