Canonical Allele Identifier: PA2825582020
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376019
ClinVar RCV Id: RCV000433391 RCV001290697
ClinVar Variation Id: 376020
ClinVar RCV Id: RCV000441948 RCV001290696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Arg135Ser
CA16602488
NM_001122607.2:c.405G>T
CA16602489
NM_001122607.2:c.405G>C