Canonical Allele Identifier: PA2828329233
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474938
ClinVar RCV Id: RCV001973749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356334.1:p.Asp449Tyr
CA363957115
NM_001369405.1:c.1345G>T