Canonical Allele Identifier: PA2825669756
Gene: USP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 528040
ClinVar RCV Id: RCV000633119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122082.1:p.Arg275Trp
CA7555572
NM_001128610.3:c.823C>T