Canonical Allele Identifier: PA915969180
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 660789
ClinVar RCV Id: RCV000818068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Asn96Ser
CA10014555
NM_001754.5:c.287A>G