Canonical Allele Identifier: PA2829184671
Gene: USP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376590.1:p.Gln450Arg
CA3059181
NM_001389661.1:c.1349A>G