Canonical Allele Identifier: PA658800564
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 500283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019801.3:p.Gln51Lys
CA3836273
NM_001024630.4:c.151C>A