Canonical Allele Identifier: PA2829480093
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 429759
ClinVar RCV Id: RCV000494135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Ser238Pro
CA363588346
NM_004159.5:c.712T>C