Canonical Allele Identifier: PA2829184478
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069011
ClinVar RCV Id: RCV002975271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376588.1:p.Gln489Leu
CA3059174
NM_001389659.1:c.1466A>T