Canonical Allele Identifier: PA2826640634
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_001269167.1:p.Gly709Arg
CA266104812
NM_001282238.2:c.2125G>C
CA2573150453
NM_001282238.2:c.2124_2125delinsTC