Canonical Allele Identifier: PA2825590814
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_001116855.1:p.Ala1280Asp
CA16608460
NM_001123383.1:c.3839C>A