Canonical Allele Identifier: PA2741972096
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2617322
ClinVar RCV Id: RCV003374224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061923.2:p.Asn286Ile
CA358030328
NM_019050.3:c.857A>T