Canonical Allele Identifier: PA2826602388
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3015674
ClinVar RCV Id: RCV003873761
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265407.1:p.Pro449Ser
CA363957251
NM_001278478.2:c.1345C>T