Canonical Allele Identifier: PA2499238180
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002692
ClinVar RCV Id: RCV001299153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Thr9Arg
CA410204303
NM_001122607.2:c.26C>G