Canonical Allele Identifier: PA645383509
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376019
ClinVar Variation Id: 376020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Arg162Ser
CA16602488
NM_001754.5:c.486G>T
CA16602489
NM_001754.5:c.486G>C