Canonical Allele Identifier: PA2829341611
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002692
ClinVar RCV Id: RCV001299153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Thr36Arg
CA410204303
NM_001754.5:c.107C>G