Canonical Allele Identifier: PA2825238582
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409816
ClinVar RCV Id: RCV000469722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Pro436Ser
CA16616503
NM_001001890.3:c.1306C>T