Canonical Allele Identifier: PA2825236618
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 463980
ClinVar RCV Id: RCV000543395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001890.1:p.Pro16Ser
CA410204228
NM_001001890.3:c.46C>T