Canonical Allele Identifier: PA658665549
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 133679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060215.4:p.Tyr985Phe
CA157293
NM_017745.6:c.2954A>T