Canonical Allele Identifier: PA2825581993
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718521
ClinVar RCV Id: RCV002296659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Thr121Ser
CA410202598
NM_001122607.2:c.362C>G
CA410202601
NM_001122607.2:c.361A>T