Canonical Allele Identifier: PA2580257300
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076125
ClinVar RCV Id: RCV002979120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Thr323Arg
CA320251671
NM_001754.5:c.968C>G