Canonical Allele Identifier: PA2573221302
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1450492
ClinVar RCV Id: RCV001990168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Pro86Leu
CA410203786
NM_001754.5:c.257C>T