Canonical Allele Identifier: PA2825310861
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 3181960
ClinVar RCV Id: RCV004471307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014839.1:p.Asp217Asn
CA760144
NM_001014839.1:c.649G>A