Canonical Allele Identifier: PA2825310991
Gene: NCDN HGNC NCBI
ClinVar RCV:
RCV003406324
ClinVar Variation:
2638648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Arg270His
CA760174
NM_001014841.1:c.809G>A