Canonical Allele Identifier: PA2829185102
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069011
ClinVar RCV Id: RCV002975271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376595.1:p.Gln373Leu
CA3059174
NM_001389666.1:c.1118A>T