Canonical Allele Identifier: PA2825581923
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722136
ClinVar RCV Id: RCV002302360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Asp57Gly
CA410203802
NM_001122607.2:c.170A>G