Canonical Allele Identifier: PA2573221337
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1364020
ClinVar RCV Id: RCV001905199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Thr148Ala
CA410202602
NM_001754.5:c.442A>G