Canonical Allele Identifier: PA2825582072
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532659
ClinVar RCV Id: RCV000639519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Thr161Ser
CA410208042
NM_001122607.2:c.482C>G
CA410208046
NM_001122607.2:c.481A>T