Canonical Allele Identifier: PA123979
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.His85Asn
CA123975
NM_001754.5:c.253C>A