Canonical Allele Identifier: PA915969127
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 639088
ClinVar RCV Id: RCV000791802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Pro57Arg
CA410204028
NM_001754.5:c.170C>G