Canonical Allele Identifier: PA2825311030
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 984914
ClinVar RCV Id: RCV001391340 RCV001526830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Trp481Arg
CA339346427
NM_001014841.1:c.1441T>A
CA339346431
NM_001014841.1:c.1441T>C