Canonical Allele Identifier: PA2826640115
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 2772976
ClinVar RCV Id: RCV003576954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269166.1:p.Pro754Leu
CA390933603
NM_001282237.2:c.2261C>T