Canonical Allele Identifier: PA2825582023
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695375
ClinVar RCV Id: RCV002264877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Phe136Leu
CA410202502
NM_001122607.2:c.408T>G
CA410202503
NM_001122607.2:c.408T>A
CA410202509
NM_001122607.2:c.406T>C