Canonical Allele Identifier: PA123978
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.His58Asn
CA123975
NM_001122607.2:c.172C>A