Canonical Allele Identifier: PA2826640178
Gene: BCL11B HGNC NCBI
ClinVar RCV:
RCV002041365
ClinVar Variation:
1346196
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269166.1:p.Asp884Asn
CA390932711
NM_001282237.2:c.2650G>A