Canonical Allele Identifier: PA206466
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 196302
ClinVar RCV Id: RCV000193162 RCV000723609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019801.3:p.Gln65_Gln71del
CA206465
NM_001024630.4:c.193_213del