Canonical Allele Identifier: PA658810403
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 531807
ClinVar RCV Id: RCV000638321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005661.1:p.Met236Val
CA149184177
NM_005670.4:c.706A>G