Canonical Allele Identifier: PA1139750026
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 963066
ClinVar RCV Id: RCV003763917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683720.2:p.Val106Met
CA363589261
NM_148919.4:c.316G>A