Canonical Allele Identifier: PA239921
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 194101
ClinVar RCV Id: RCV000174383 RCV001078522 RCV002336422 RCV004552962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116855.1:p.Met1541Thr
CA239918
NM_001123383.1:c.4622T>C