Canonical Allele Identifier: PA2741825881
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3015674
ClinVar RCV Id: RCV003873761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019801.3:p.Pro485Ser
CA363957251
NM_001024630.4:c.1453C>T