Canonical Allele Identifier: PA2829184847
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376592.1:p.Gln385Arg
CA3059181
NM_001389663.1:c.1154A>G