Canonical Allele Identifier: PA1139676157
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 971877
ClinVar RCV Id: RCV001247761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Thr84Ile
CA10014550
NM_001122607.2:c.251C>T