Canonical Allele Identifier: PA2742024361
Gene: CUX1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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