Canonical Allele Identifier: PA2829928149
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061923.2:p.Val49Asp
CA358022181
NM_019050.3:c.146T>A