Canonical Allele Identifier: PA2829359230
Gene: CUX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2517260
ClinVar RCV Id: RCV003274409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001904.2:p.Val287Met
CA4410622
NM_001913.5:c.859G>A