Canonical Allele Identifier: PA2825581911
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 859484
ClinVar RCV Id: RCV001065607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Met51Thr
CA410203840
NM_001122607.2:c.152T>C