Canonical Allele Identifier: PA2741833769
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 2849117
ClinVar RCV Id: RCV003623198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116857.1:p.Arg1217_Glu1219del
CA2739273433
NM_001123385.2:c.3648_3656del