Canonical Allele Identifier: PA645383488
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436617
ClinVar RCV Id: RCV000502317 RCV000824706
ClinVar Variation Id: 1045299
ClinVar RCV Id: RCV001349685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Trp106Arg
CA410203507
NM_001754.5:c.316T>C
CA410203508
NM_001754.5:c.316T>A