Canonical Allele Identifier: PA891850986
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 581279
ClinVar RCV Id: RCV000705057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Asn136Lys
CA410202676
NM_001754.5:c.408T>G
CA410202677
NM_001754.5:c.408T>A