Canonical Allele Identifier: PA2580547561
Gene: CUX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2400500
ClinVar RCV Id: RCV002734563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_852477.1:p.Ala204Thr
CA4410520
NM_181500.4:c.610G>A