Canonical Allele Identifier: PA2741963783
Gene: BCOR HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060215.4:p.Arg342Gly
CA327993585
NM_017745.6:c.1024C>G