Canonical Allele Identifier: PA2825582035
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 561243
ClinVar RCV Id: RCV000680415 RCV000824705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Gly141Arg
CA410202478
NM_001122607.2:c.421G>C
CA410202479
NM_001122607.2:c.421G>A