Canonical Allele Identifier: PA2830001017
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 1423766
ClinVar RCV Id: RCV001954890
ClinVar Variation Id: 1522892
ClinVar RCV Id: RCV002036348
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075049.1:p.Gly710Arg
CA266104812
NM_022898.3:c.2128G>C
CA2573150453
NM_022898.3:c.2127_2128delinsTC