Canonical Allele Identifier: PA1139676132
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 856798
ClinVar RCV Id: RCV001062338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Arg80Ser
CA410203493
NM_001122607.2:c.238C>A