Canonical Allele Identifier: PA2829928168
Gene: USP53 HGNC NCBI
ClinVar RCV:
RCV004477607
ClinVar Variation:
3187764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061923.2:p.Gln501Arg
CA3059181
NM_019050.3:c.1502A>G