Canonical Allele Identifier: PA2742004173
Gene: BCL11B HGNC NCBI
ClinVar RCV:
RCV003576954
ClinVar Variation:
2772976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612808.1:p.Pro755Leu
CA390933603
NM_138576.4:c.2264C>T