Canonical Allele Identifier: PA645373868
Gene: RUNX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 257095
ClinVar RCV Id: RCV000243178 RCV000956383 RCV000987708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019801.3:p.Ala84_Ala89del
CA3836310
NM_001024630.4:c.243_260del
CA1088530216
NM_001024630.4:c.246_263del
CA2578634849
NM_001024630.4:c.249_266del