Canonical Allele Identifier: PA112089
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 417961
ClinVar RCV Id: RCV000477937 RCV001270105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Arg139Gln
CA16616941
NM_001001890.3:c.416G>A