Canonical Allele Identifier: PA2828329229
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 634441
ClinVar RCV Id: RCV000784916 RCV000784915 RCV001869165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356334.1:p.Pro446Leu
CA3836615
NM_001369405.1:c.1337C>T