Canonical Allele Identifier: PA2825236580
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002692
ClinVar RCV Id: RCV001299153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Thr9Arg
CA410204303
NM_001001890.3:c.26C>G