Canonical Allele Identifier: PA658810003
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532660
ClinVar RCV Id: RCV000639520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Asn434Ser
CA10014187
NM_001754.5:c.1301A>G