Canonical Allele Identifier: PA2825581902
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 649413
ClinVar RCV Id: RCV000804342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Gly47Arg
CA410203869
NM_001122607.2:c.139G>C