Canonical Allele Identifier: PA2580371921
Gene: NCDN HGNC NCBI
ClinVar RCV:
RCV002262228
ClinVar Variation:
1694508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055099.1:p.Thr713Met
CA760405
NM_014284.3:c.2138C>T