Canonical Allele Identifier: PA2828483638
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3065121
ClinVar RCV Id: RCV003990198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358327.1:p.Val49Asp
CA358022181
NM_001371398.1:c.146T>A