Canonical Allele Identifier: PA2825590566
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 2826046
ClinVar RCV Id: RCV003622833
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116855.1:p.Ser834Gly
CA412742514
NM_001123383.1:c.2500A>G