Canonical Allele Identifier: PA658809939
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532659
ClinVar RCV Id: RCV000639519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Thr188Ser
CA410208042
NM_001754.5:c.563C>G
CA410208046
NM_001754.5:c.562A>T