Canonical Allele Identifier: PA248632
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14471
ClinVar RCV Id: RCV000015558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Ala156Glu
CA248628
NM_001754.5:c.467C>A