Canonical Allele Identifier: PA2825581929
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003438
ClinVar RCV Id: RCV001299989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Pro59Ala
CA320642689
NM_001122607.2:c.175C>G