Canonical Allele Identifier: PA2829184532
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 619050
ClinVar RCV Id: RCV000766148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376589.1:p.Arg58Gln
CA3058833
NM_001389660.1:c.173G>A