Canonical Allele Identifier: PA2499278254
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 984913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055099.1:p.Arg478Gln
CA339346242
NM_014284.3:c.1433G>A