Canonical Allele Identifier: PA2829184329
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2305117
ClinVar RCV Id: RCV002895954
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376587.1:p.Leu93Phe
CA3058868
NM_001389658.1:c.277C>T