Canonical Allele Identifier: PA2830398111
Gene: CUX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2211884
ClinVar RCV Id: RCV002660348
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_853530.2:p.Ala294Thr
CA4410655
NM_181552.4:c.880G>A