Canonical Allele Identifier: PA2830001102
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 1346196
ClinVar RCV Id: RCV002041365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075049.1:p.Asp814Asn
CA390932711
NM_022898.3:c.2440G>A