Canonical Allele Identifier: PA2828328984
Gene: RUNX2 HGNC NCBI
ClinVar RCV:
RCV002572833
ClinVar Variation:
1902600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356334.1:p.Ile3Phe
CA3836248
NM_001369405.1:c.7A>T