Canonical Allele Identifier: PA290743
Gene: EOMES HGNC NCBI

Linked Data

ClinVar Variation Id: 137212
ClinVar RCV Id: RCV000124893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005433.2:p.Ala120Gly
CA290741
NM_005442.4:c.359C>G