Canonical Allele Identifier: PA2825591472
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_001116856.1:p.Arg1165_Glu1167del
CA2739273433
NM_001123384.2:c.3492_3500del