Allele Registry

Canonical Allele Identifier: PA2825311002

Gene: NCDN HGNC NCBI

ClinVar RCV:

RCV003402796

ClinVar Variation:

2635255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001014841.1:p.Thr318Ser	CA339344592 NM_001014841.1:c.952A>T CA339344594 NM_001014841.1:c.953C>G