Canonical Allele Identifier: PA2829479992
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 649739
ClinVar RCV Id: RCV000804736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Cys120Ser
CA3746403
NM_004159.5:c.359G>C
CA363589139
NM_004159.5:c.358T>A