Canonical Allele Identifier: PA2825669813
Gene: USP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161991
ClinVar RCV Id: RCV000149416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122082.1:p.Ser719del
CA174935
NM_001128610.3:c.2155_2157del