Canonical Allele Identifier: PA1139705702
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 956982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Asn159Asp
CA410202533
NM_001754.5:c.475A>G