Canonical Allele Identifier: PA2830393073
Gene: CUX1 HGNC NCBI
ClinVar RCV:
RCV002660348
ClinVar Variation:
2211884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852477.1:p.Ala303Thr
CA4410655
NM_181500.4:c.907G>A