Canonical Allele Identifier: PA2499236098
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 1299180
ClinVar RCV Id: RCV001727510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034680.2:p.Ile2404Thr
CA412752509
NM_001039591.3:c.7211T>C