Canonical Allele Identifier: PA2829877194
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 133694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060215.4:p.Arg1234Gly
CA157363
NM_017745.6:c.3700A>G