Canonical Allele Identifier: PA2825311060
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 1694508
ClinVar RCV Id: RCV002262228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Thr696Met
CA760405
NM_001014841.1:c.2087C>T