Canonical Allele Identifier: PA2829877216
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_060215.4:p.Ala1280Asp
CA16608460
NM_017745.6:c.3839C>A