Canonical Allele Identifier: PA2580371913
Gene: NCDN HGNC NCBI
ClinVar RCV:
RCV004255362
ClinVar Variation:
2461748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055099.1:p.Arg259Trp
CA760164
NM_014284.3:c.775C>T