Canonical Allele Identifier: PA2829184572
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2589073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376589.1:p.Leu435Pro
CA3059173
NM_001389660.1:c.1304T>C