Canonical Allele Identifier: PA2829479990
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 870500
ClinVar RCV Id: RCV001093597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Asp119Asn
CA363589149
NM_004159.5:c.355G>A