Canonical Allele Identifier: PA2829317709
Gene: USP28 HGNC NCBI

Linked Data

ClinVar Variation Id: 161740
ClinVar RCV Id: RCV000149276
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387715.1:p.Leu191Phe
CA174700
NM_001400786.1:c.571C>T