Canonical Allele Identifier: PA645383673
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 339874
ClinVar RCV Id: RCV000272599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Glu474Asp
CA10652929
NM_001754.5:c.1422G>T
CA410146637
NM_001754.5:c.1422G>C