Canonical Allele Identifier: PA915969186
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 660172
ClinVar RCV Id: RCV000817304
ClinVar Variation Id: 864271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Glu138Asp
CA10014520
NM_001754.5:c.414A>C
CA320638000
NM_001754.5:c.414A>T