Canonical Allele Identifier: PA2825310995
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 3181982
ClinVar RCV Id: RCV004471329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Arg302Gln
CA760192
NM_001014841.1:c.905G>A