Canonical Allele Identifier: PA645464018
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 254673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612808.1:p.Asn441Lys
CA10586691
NM_138576.4:c.1323T>G
CA390935639
NM_138576.4:c.1323T>A