Canonical Allele Identifier: PA2825310986
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 2461748
ClinVar RCV Id: RCV004255362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Arg242Trp
CA760164
NM_001014841.1:c.724C>T