Canonical Allele Identifier: PA112099
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14464
ClinVar RCV Id: RCV000015550 RCV000680425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Arg174Gln
CA248610
NM_001001890.3:c.521G>A