Canonical Allele Identifier: PA2825310912
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 984913
ClinVar RCV Id: RCV001391339 RCV001526832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014839.1:p.Arg478Gln
CA339346242
NM_001014839.1:c.1433G>A