Allele Registry

Canonical Allele Identifier: PA2499273769

Gene: NCOR2 HGNC NCBI

ClinVar RCV:

RCV001688152

RCV003975987

ClinVar Variation:

1278544

HGVS (amino-acid)	Matching Registered Transcripts
NP_006303.4:p.Ala1699Thr	CA6868078 NM_006312.6:c.5095G>A