Canonical Allele Identifier: PA2826640664
Gene: BCL11B HGNC NCBI

Linked Data

ClinVar Variation Id: 1164020
ClinVar RCV Id: RCV001726571 RCV001788503 RCV004007233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269167.1:p.Ser764Asn
CA390933062
NM_001282238.2:c.2291G>A