Canonical Allele Identifier: PA2825311013
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 984912
ClinVar RCV Id: RCV001391338 RCV001526833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Glu416Gln
CA339345943
NM_001014841.1:c.1246G>C