Canonical Allele Identifier: PA2825310974
Gene: NCDN HGNC NCBI
ClinVar RCV:
RCV004471307
ClinVar Variation:
3181960
JSON-LD

Amino-acid Alleles

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