Canonical Allele Identifier: PA2829184355
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376587.1:p.Ala306Thr
CA358030573
NM_001389658.1:c.916G>A