Canonical Allele Identifier: PA645484377
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 422179
ClinVar RCV Id: RCV000482190
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034679.2:p.Trp435Arg
CA16621373
NM_001039590.3:c.1303T>C
CA412770007
NM_001039590.3:c.1303T>A