Canonical Allele Identifier: PA2829877172
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 2849117
ClinVar RCV Id: RCV003623198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060215.4:p.Arg1183_Glu1185del
CA2739273433
NM_017745.6:c.3546_3554del