Canonical Allele Identifier: PA2825581932
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422929
ClinVar RCV Id: RCV001926349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Gly60Asn
CA2573157361
NM_001122607.2:c.178_179delinsAA