Canonical Allele Identifier: PA2825581999
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713291
ClinVar RCV Id: RCV002302875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Ala123Asp
CA410202586
NM_001122607.2:c.368C>A