Canonical Allele Identifier: PA1139705528
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 934627
ClinVar RCV Id: RCV001203054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Asp33Tyr
CA410205635
NM_001754.5:c.97G>T