Canonical Allele Identifier: PA916078556
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 649739
ClinVar RCV Id: RCV000804736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Cys124Ser
CA3746403
NM_148919.4:c.371G>C
CA363589139
NM_148919.4:c.370T>A