Canonical Allele Identifier: PA2829479934
Gene: PSMB8 HGNC NCBI

Linked Data

ClinVar Variation Id: 643533
ClinVar RCV Id: RCV000797256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004150.1:p.Phe76Leu
CA3746456
NM_004159.5:c.228C>G
CA363589427
NM_004159.5:c.228C>A
CA363589431
NM_004159.5:c.226T>C