Canonical Allele Identifier: PA2825236729
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000965
ClinVar RCV Id: RCV001297178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Ala33Pro
CA410204003
NM_001001890.3:c.97G>C