Canonical Allele Identifier: PA2829479984
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047832
ClinVar RCV Id: RCV003771027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Met113Ile
CA3746407
NM_004159.5:c.339G>A
CA363589183
NM_004159.5:c.339G>T
CA363589184
NM_004159.5:c.339G>C