Canonical Allele Identifier: PA891850988
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 566052
ClinVar RCV Id: RCV000685769 RCV002485591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Ser141Ala
CA410202644
NM_001754.5:c.421T>G