Canonical Allele Identifier: PA2829184759
Gene: USP53 HGNC NCBI
ClinVar RCV:
RCV004477607
ClinVar Variation:
3187764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376591.1:p.Gln385Arg
CA3059181
NM_001389662.1:c.1154A>G