Canonical Allele Identifier: PA2826640387
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 254673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269167.1:p.Asn369Lys
CA10586691
NM_001282238.2:c.1107T>G
CA390935639
NM_001282238.2:c.1107T>A