Canonical Allele Identifier: PA2825237022
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436617
ClinVar Variation Id: 1045299
ClinVar RCV Id: RCV001349685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Trp79Arg
CA410203507
NM_001001890.3:c.235T>C
CA410203508
NM_001001890.3:c.235T>A