Allele Registry

Canonical Allele Identifier: PA2825591565

Gene: BCOR HGNC NCBI

ClinVar RCV:

RCV000454264

RCV002248664

RCV003989531

ClinVar Variation:

402203

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116856.1:p.Ser1379Tyr	CA10386468 NM_001123384.2:c.4136C>A