Canonical Allele Identifier: PA2826640128
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 1423766
ClinVar RCV Id: RCV001954890
ClinVar Variation Id: 1522892
ClinVar RCV Id: RCV002036348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269166.1:p.Gly780Arg
CA266104812
NM_001282237.2:c.2338G>C
CA2573150453
NM_001282237.2:c.2337_2338delinsTC