Canonical Allele Identifier: PA2829184813
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1903044
ClinVar RCV Id: RCV002583395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376592.1:p.Ser69Phe
CA3058946
NM_001389663.1:c.206C>T