Allele Registry

Canonical Allele Identifier: PA2825590850

Gene: BCOR HGNC NCBI

ClinVar RCV:

RCV000454264

RCV002248664

RCV003989531

ClinVar Variation:

402203

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116855.1:p.Ser1397Tyr	CA10386468 NM_001123383.1:c.4190C>A