Canonical Allele Identifier: PA2825590969
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 521361
ClinVar RCV Id: RCV000622518 RCV001528742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116855.1:p.Asp1678Asn
CA10386293
NM_001123383.1:c.5032G>A