Canonical Allele Identifier: PA2825311028
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 2434074
ClinVar RCV Id: RCV003132856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Phe477Leu
CA339346376
NM_001014841.1:c.1429T>C
CA339346387
NM_001014841.1:c.1431C>A
CA339346389
NM_001014841.1:c.1431C>G