Canonical Allele Identifier: PA2829184930
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2976007
ClinVar RCV Id: RCV003834093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376593.1:p.Asp366His
CA3059171
NM_001389664.1:c.1096G>C