Canonical Allele Identifier: PA2742024361
Gene: CUX1 HGNC NCBI
ClinVar RCV:
RCV003274409
ClinVar Variation:
2517260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852477.1:p.Val287Met
CA4410622
NM_181500.4:c.859G>A