ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826262702
Gene: CUX1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000880414
RCV003940410
ClinVar Variation:
709065
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001189474.1:p.Val99Ile
CA4410396
NM_001202545.3:c.295G>A