Canonical Allele Identifier: PA2741825879
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_001019801.3:p.Gly461Arg
CA3836618
NM_001024630.4:c.1381G>C
CA363957103
NM_001024630.4:c.1381G>A