Canonical Allele Identifier: PA290742
Gene: EOMES HGNC NCBI

Linked Data

ClinVar Variation Id: 137212
ClinVar RCV Id: RCV000124893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265111.1:p.Ala120Gly
CA290741
NM_001278182.2:c.359C>G