Canonical Allele Identifier: PA2825581869
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000965
ClinVar RCV Id: RCV001297178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Ala33Pro
CA410204003
NM_001122607.2:c.97G>C