Canonical Allele Identifier: PA2830290085
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3220941
ClinVar RCV Id: RCV004515818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Ser118Pro
CA363589181
NM_148919.4:c.352T>C