Canonical Allele Identifier: PA2826602157
Gene: RUNX2 HGNC NCBI
ClinVar RCV:
RCV000009882
ClinVar Variation:
9299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265407.1:p.Ser177Asn
CA280137
NM_001278478.2:c.530G>A