Canonical Allele Identifier: PA2830442158
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_955475.1:p.His777Tyr
CA352780499
NM_199443.3:c.2329C>T