Canonical Allele Identifier: PA2829184820
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2617322
ClinVar RCV Id: RCV003374224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376592.1:p.Asn170Ile
CA358030328
NM_001389663.1:c.509A>T