Canonical Allele Identifier: PA2825582033
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1351602
ClinVar RCV Id: RCV002044851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Ser140Thr
CA410202484
NM_001122607.2:c.419G>C