Canonical Allele Identifier: PA891859575
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 568159
ClinVar RCV Id: RCV000688424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Ser56Cys
CA137008158
NM_148919.4:c.167C>G
CA891842687
NM_148919.4:c.167_168delinsGT