Canonical Allele Identifier: PA1139705683
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 949250
ClinVar RCV Id: RCV001220670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Asn146Tyr
CA410202614
NM_001754.5:c.436A>T