Canonical Allele Identifier: PA2826602269
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312166
ClinVar RCV Id: RCV001752819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265407.1:p.Tyr285Cys
CA363955902
NM_001278478.2:c.854A>G