Canonical Allele Identifier: PA2825581832
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 463980
ClinVar RCV Id: RCV000543395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116079.1:p.Pro16Ser
CA410204228
NM_001122607.2:c.46C>T