Canonical Allele Identifier: PA2825236835
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037898
ClinVar RCV Id: RCV001341123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Ser46Arg
CA410203871
NM_001001890.3:c.138C>G
CA410203872
NM_001001890.3:c.138C>A
CA410203878
NM_001001890.3:c.136A>C