Canonical Allele Identifier: PA2826602382
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2966454
ClinVar RCV Id: RCV003821068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265407.1:p.Thr445Met
CA3836633
NM_001278478.2:c.1334C>T