Canonical Allele Identifier: PA2580371917
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 2323585
ClinVar RCV Id: RCV004164981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055099.1:p.Pro452Arg
CA339346070
NM_014284.3:c.1355C>G