Canonical Allele Identifier: PA915969119
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 641583
ClinVar RCV Id: RCV000794855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Ser53Gly
CA410204087
NM_001754.5:c.157A>G