Canonical Allele Identifier: PA2825237376
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532659
ClinVar RCV Id: RCV000639519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Thr161Ser
CA410208042
NM_001001890.3:c.482C>G
CA410208046
NM_001001890.3:c.481A>T