Canonical Allele Identifier: PA2826601804
Gene: RUNX2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265407.1:p.Ile3Phe
CA3836248
NM_001278478.2:c.7A>T