Canonical Allele Identifier: PA2829184373
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2589073
ClinVar RCV Id: RCV003363281 RCV003699070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376587.1:p.Leu485Pro
CA3059173
NM_001389658.1:c.1454T>C