Canonical Allele Identifier: PA2741943029
Gene: NCDN HGNC NCBI
ClinVar RCV:
RCV003402796
ClinVar Variation:
2635255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055099.1:p.Thr335Ser
CA339344592
NM_014284.3:c.1003A>T
CA339344594
NM_014284.3:c.1004C>G