Canonical Allele Identifier: PA2573297652
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_612808.1:p.Asp885Asn
CA390932711
NM_138576.4:c.2653G>A