Canonical Allele Identifier: PA891850970
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 576717
ClinVar RCV Id: RCV000699282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Arg76Cys
CA410203854
NM_001754.5:c.226C>T