Allele Registry

Canonical Allele Identifier: PA2830001079

Gene: BCL11B HGNC NCBI

ClinVar RCV:

RCV001726571

RCV001788503

RCV004007233

ClinVar Variation:

1164020

HGVS (amino-acid)	Matching Registered Transcripts
NP_075049.1:p.Ser765Asn	CA390933062 NM_022898.3:c.2294G>A