Canonical Allele Identifier: PA2828284029
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 462932
ClinVar RCV Id: RCV000525708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355058.1:p.Pro60Ala
CA366191121
NM_001368129.2:c.178C>G