Canonical Allele Identifier: PA2825669810
Gene: USP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379085
ClinVar RCV Id: RCV001883586 RCV002490098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122082.1:p.Pro703His
CA7555893
NM_001128610.3:c.2108C>A