Canonical Allele Identifier: PA2741833468
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2844927
ClinVar RCV Id: RCV003630792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Trp79Cys
CA410203495
NM_001122607.2:c.237G>T
CA410203498
NM_001122607.2:c.237G>C