Canonical Allele Identifier: PA2826006955
Gene: EMX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 499434
ClinVar RCV Id: RCV000596975 RCV001255078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159396.1:p.Ala58_Ala59dup
CA5711387
NM_001165924.2:c.173_178dup