Allele Registry

Canonical Allele Identifier: PA101446

Gene: BCOR HGNC NCBI

ClinVar RCV:

RCV000011658

RCV001545250

ClinVar Variation:

10911

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116857.1:p.Pro85Leu	CA340996 NM_001123385.2:c.254C>T