Canonical Allele Identifier: PA2829184458
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2318909
ClinVar RCV Id: RCV002915268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376588.1:p.Ala306Thr
CA358030573
NM_001389659.1:c.916G>A