Canonical Allele Identifier: PA2829184549
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1903044
ClinVar RCV Id: RCV002583395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376589.1:p.Ser185Phe
CA3058946
NM_001389660.1:c.554C>T