Allele Registry

Canonical Allele Identifier: PA2829184631

Gene: USP53 HGNC NCBI

ClinVar RCV:

RCV002897079

RCV003561119

ClinVar Variation:

2313908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001376590.1:p.Asn97Asp	CA3058871 NM_001389661.1:c.289A>G