Canonical Allele Identifier: PA2825590762
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 2849117
ClinVar RCV Id: RCV003623198
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116855.1:p.Arg1183_Glu1185del
CA2739273433
NM_001123383.1:c.3546_3554del