Canonical Allele Identifier: PA2825313100
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_001015051.3:p.Asp441Tyr
CA363957115
NM_001015051.4:c.1321G>T