Allele Registry

Canonical Allele Identifier: PA2580371919

Gene: NCDN HGNC NCBI

ClinVar Variation Id: 2434074

HGVS (amino-acid)	Matching Registered Transcripts
NP_055099.1:p.Phe494Leu	CA339346376 NM_014284.3:c.1480T>C CA339346387 NM_014284.3:c.1482C>A CA339346389 NM_014284.3:c.1482C>G