Canonical Allele Identifier: PA2826342539
Gene: USP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2546331
ClinVar RCV Id: RCV004315093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001238806.1:p.Ser157Cys
CA352774134
NM_001251877.2:c.469A>T