Canonical Allele Identifier: PA2830000381
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 254673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075049.1:p.Asn370Lys
CA10586691
NM_022898.3:c.1110T>G
CA390935639
NM_022898.3:c.1110T>A