Canonical Allele Identifier: PA2825582032
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2443682
ClinVar RCV Id: RCV003152289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Ser140Gly
CA410202486
NM_001122607.2:c.418A>G