Canonical Allele Identifier: PA2830398127
Gene: CUX1 HGNC NCBI
ClinVar RCV:
RCV003434049
ClinVar Variation:
2657861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_853530.2:p.Pro430Ala
CA4410826
NM_181552.4:c.1288C>G