Canonical Allele Identifier: PA174940
Gene: USP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161993
ClinVar RCV Id: RCV000149418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005145.3:p.Ser718Cys
CA174939
NM_005154.5:c.2153C>G