Canonical Allele Identifier: PA1139705543
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 949338
ClinVar RCV Id: RCV001220776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Pro49Thr
CA320642967
NM_001754.5:c.145C>A