Canonical Allele Identifier: PA2826262728
Gene: CUX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2211884
ClinVar RCV Id: RCV002660348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189474.1:p.Ala259Thr
CA4410655
NM_001202545.3:c.775G>A