Canonical Allele Identifier: PA2828483381
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358325.1:p.Gln438Leu
CA3059174
NM_001371396.1:c.1313A>T