Canonical Allele Identifier: PA2825591388
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 133679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116856.1:p.Tyr985Phe
CA157293
NM_001123384.2:c.2954A>T