Canonical Allele Identifier: PA2829479915
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 465420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Thr70Ser
CA3746460
NM_004159.5:c.208A>T
CA137008119
NM_004159.5:c.208_210delinsTCA
CA363589465
NM_004159.5:c.209C>G