Canonical Allele Identifier: PA2828329231
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2714726
ClinVar RCV Id: RCV003552978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356334.1:p.Gly447Arg
CA3836618
NM_001369405.1:c.1339G>C
CA363957103
NM_001369405.1:c.1339G>A