Canonical Allele Identifier: PA2829447999
Gene: USP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3187579
ClinVar RCV Id: RCV004477422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003354.2:p.His824Tyr
CA352780499
NM_003363.4:c.2470C>T