Canonical Allele Identifier: PA2825385638
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 2856688
ClinVar RCV Id: RCV003696544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034679.2:p.Asp2497Glu
CA412754376
NM_001039590.3:c.7491C>A
CA412754378
NM_001039590.3:c.7491C>G