Canonical Allele Identifier: PA2826602013
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_001265407.1:p.Ala70_Ala75del
CA3836310
NM_001278478.2:c.201_218del
CA1088530216
NM_001278478.2:c.204_221del
CA2578634849
NM_001278478.2:c.207_224del