Canonical Allele Identifier: PA2829185099
Gene: USP53 HGNC NCBI
ClinVar RCV:
RCV003834093
ClinVar Variation:
2976007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376595.1:p.Asp366His
CA3059171
NM_001389666.1:c.1096G>C