Canonical Allele Identifier: PA915969107
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_001745.2:p.Thr41Met
CA10014590
NM_001754.5:c.122C>T