Canonical Allele Identifier: PA2825311049
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 984915
ClinVar RCV Id: RCV001391341 RCV001526831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Pro635Leu
CA339349113
NM_001014841.1:c.1904C>T