Canonical Allele Identifier: PA2825310883
Gene: NCDN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014839.1:p.Arg287His
CA760174
NM_001014839.1:c.860G>A