Canonical Allele Identifier: PA915958208
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 422179
ClinVar RCV Id: RCV000482190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034680.2:p.Trp435Arg
CA16621373
NM_001039591.3:c.1303T>C
CA412770007
NM_001039591.3:c.1303T>A