Canonical Allele Identifier: PA2580433019
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2318909
ClinVar RCV Id: RCV002915268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061923.2:p.Ala306Thr
CA358030573
NM_019050.3:c.916G>A