Canonical Allele Identifier: PA658809928
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532671
ClinVar RCV Id: RCV000639531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Thr111Ala
CA410203415
NM_001754.5:c.331A>G