Canonical Allele Identifier: PA2825591513
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 390714
ClinVar RCV Id: RCV000440434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116856.1:p.Ala1262Asp
CA16608460
NM_001123384.2:c.3785C>A