Canonical Allele Identifier: PA2825591942
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 265045
ClinVar RCV Id: RCV000254917 RCV004021021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116857.1:p.Arg763Trp
CA10386811
NM_001123385.2:c.2287C>T