Canonical Allele Identifier: PA2741833472
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_001116079.1:p.Thr84Ser
CA410203410
NM_001122607.2:c.251C>G
CA410203414
NM_001122607.2:c.250A>T