Canonical Allele Identifier: PA157367
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 133694
ClinVar RCV Id: RCV000120222 RCV000862923 RCV004551184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116857.1:p.Arg1268Gly
CA157363
NM_001123385.2:c.3802A>G