Canonical Allele Identifier: PA2825236602
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 661459
ClinVar RCV Id: RCV000818880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Thr14Met
CA10014590
NM_001001890.3:c.41C>T