ClinGen Allele Registry
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Canonical Allele Identifier:
PA113729
Gene: RUNX2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000009885
RCV000731332
RCV002482851
RCV003934819
ClinVar Variation:
9302
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001019801.3:p.Arg225Gln
CA280138
NM_001024630.4:c.674G>A