Canonical Allele Identifier: PA2829184913
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2318909
ClinVar RCV Id: RCV002915268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376593.1:p.Ala190Thr
CA358030573
NM_001389664.1:c.568G>A