ClinGen Allele Registry
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Canonical Allele Identifier:
PA1139677073
Gene: USP9X
HGNC
NCBI
Linked Data
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001034680.2:p.Leu174del
NM_001039591.3:c.520_522del
NM_001039591.3:c.[520_522del;525C>A]
NM_001039591.3:c.[520_522del;525C=]
NM_001039591.3:c.[520_522del;525C>G]
NM_001039591.3:c.[520_522del;525C>T]