Canonical Allele Identifier: PA2825311017
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 2323585
ClinVar RCV Id: RCV004164981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Pro435Arg
CA339346070
NM_001014841.1:c.1304C>G