Canonical Allele Identifier: PA2829341679
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439732
ClinVar RCV Id: RCV001936692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001745.2:p.Val118Leu
CA410202790
NM_001754.5:c.352G>T
CA410202791
NM_001754.5:c.352G>C