Canonical Allele Identifier: PA2829184478
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376588.1:p.Gln489Leu
CA3059174
NM_001389659.1:c.1466A>T