Canonical Allele Identifier: PA2826602401
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 357096
ClinVar RCV Id: RCV000335280 RCV000514756 RCV002504174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265407.1:p.Gly475Ser
CA3836643
NM_001278478.2:c.1423G>A