Canonical Allele Identifier: PA915958190
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 384085
ClinVar RCV Id: RCV000428274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034680.2:p.Asn188Asp
CA10388326
NM_001039591.3:c.562A>G