Canonical Allele Identifier: PA123977
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.His58Asn
CA123975
NM_001001890.3:c.172C>A