Allele Registry

Canonical Allele Identifier: PA2829877264

Gene: BCOR HGNC NCBI

ClinVar RCV:

RCV000454264

RCV002248664

RCV003989531

ClinVar Variation:

402203

HGVS (amino-acid)	Matching Registered Transcripts
NP_060215.4:p.Ser1397Tyr	CA10386468 NM_017745.6:c.4190C>A