Canonical Allele Identifier: PA2825669814
Gene: USP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161993
ClinVar RCV Id: RCV000149418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122082.1:p.Ser718Cys
CA174939
NM_001128610.3:c.2153C>G