Canonical Allele Identifier: PA645383669
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409816
ClinVar RCV Id: RCV000469722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Pro463Ser
CA16616503
NM_001754.5:c.1387C>T