Canonical Allele Identifier: PA645400092
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 429759
ClinVar RCV Id: RCV000494135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Ser242Pro
CA363588346
NM_148919.4:c.724T>C