Allele Registry

Canonical Allele Identifier: PA2826285038

Gene: NCOR2 HGNC NCBI

ClinVar RCV:

RCV001688152

RCV003975987

ClinVar Variation:

1278544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193583.1:p.Ala1689Thr	CA6868078 NM_001206654.2:c.5065G>A