Canonical Allele Identifier: PA2580371921
Gene: NCDN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055099.1:p.Thr713Met
CA760405
NM_014284.3:c.2138C>T