Canonical Allele Identifier: PA2825236628
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2115774
ClinVar RCV Id: RCV003024386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Thr18Ala
CA410204209
NM_001001890.3:c.52A>G