Canonical Allele Identifier: PA915976963
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 656386
ClinVar RCV Id: RCV000812791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Ser8Arg
CA410204308
NM_001122607.2:c.24C>G
CA410204309
NM_001122607.2:c.24C>A
CA410204313
NM_001122607.2:c.22A>C