Canonical Allele Identifier: PA2573179807
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514344
ClinVar RCV Id: RCV002048240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Val92Ala
CA410202782
NM_001122607.2:c.275T>C