Canonical Allele Identifier: PA2825591968
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 2826046
ClinVar RCV Id: RCV003622833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116857.1:p.Ser834Gly
CA412742514
NM_001123385.2:c.2500A>G