Canonical Allele Identifier: PA2828329016
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 500283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356334.1:p.Gln37Lys
CA3836273
NM_001369405.1:c.109C>A