Allele Registry

Canonical Allele Identifier: PA2825590352

Gene: BCOR HGNC NCBI

ClinVar Allele:

2875516

ClinVar RCV:

RCV003510817

ClinVar Variation:

2713218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116855.1:p.Arg342Gly	CA327993585 NM_001123383.1:c.1024C>G