Canonical Allele Identifier: PA2825310974
Gene: NCDN HGNC NCBI

Linked Data

ClinVar Variation Id: 3181960
ClinVar RCV Id: RCV004471307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014841.1:p.Asp200Asn
CA760144
NM_001014841.1:c.598G>A