Canonical Allele Identifier: PA2825581989
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 949250
ClinVar RCV Id: RCV001220670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Asn119Tyr
CA410202614
NM_001122607.2:c.355A>T