Canonical Allele Identifier: PA229231
Gene: USP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 101078
ClinVar RCV Id: RCV000087331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122082.1:p.Gln310Lys
CA229229
NM_001128610.3:c.928C>A