Canonical Allele Identifier: PA2829184725
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376591.1:p.Ser69Phe
CA3058946
NM_001389662.1:c.206C>T