Canonical Allele Identifier: PA2829184322
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_001376587.1:p.Val49Asp
CA358022181
NM_001389658.1:c.146T>A