Allele Registry

Canonical Allele Identifier: PA2499297027

Gene: BCL11B HGNC NCBI

ClinVar RCV:

RCV001726571

RCV001788503

RCV004007233

ClinVar Variation:

1164020

HGVS (amino-acid)	Matching Registered Transcripts
NP_612808.1:p.Ser836Asn	CA390933062 NM_138576.4:c.2507G>A