Canonical Allele Identifier: PA2828483872
Gene: USP53 HGNC NCBI
ClinVar RCV:
RCV003374224
ClinVar Variation:
2617322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358328.1:p.Asn286Ile
CA358030328
NM_001371399.1:c.857A>T