Canonical Allele Identifier: PA2829341663
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2834717
ClinVar RCV Id: RCV003630619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Thr111Ser
CA410203410
NM_001754.5:c.332C>G
CA410203414
NM_001754.5:c.331A>T