Canonical Allele Identifier: PA2825237001
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2073628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Thr77Ala
CA410203539
NM_001001890.3:c.229A>G