Canonical Allele Identifier: PA2825310964
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 2470781
ClinVar RCV Id: RCV004257275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Arg131Cys
CA339343408
NM_001014841.1:c.391C>T