Canonical Allele Identifier: PA2828483469
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358326.1:p.Val49Asp
CA358022181
NM_001371397.1:c.146T>A