Canonical Allele Identifier: PA2825582042
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338528
ClinVar RCV Id: RCV001817899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Gly143Arg
CA410202465
NM_001122607.2:c.427G>A
CA410202466
NM_001122607.2:c.427G>C