Canonical Allele Identifier: PA2826682726
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_001269978.1:p.Pro597His
CA7555893
NM_001283049.1:c.1790C>A