Canonical Allele Identifier: PA2829479975
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 963066
ClinVar RCV Id: RCV003763917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Val102Met
CA363589261
NM_004159.5:c.304G>A