Canonical Allele Identifier: PA2573217440
Gene: USP28 HGNC NCBI

Linked Data

ClinVar Variation Id: 161740
ClinVar RCV Id: RCV000149276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387739.1:p.Leu66Phe
CA174700
NM_001400810.1:c.196C>T