Canonical Allele Identifier: PA645373893
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_001019801.3:p.Gly511Ser
CA3836643
NM_001024630.4:c.1531G>A