Canonical Allele Identifier: PA2829185099
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376595.1:p.Asp366His
CA3059171
NM_001389666.1:c.1096G>C