Canonical Allele Identifier: PA2828058725
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_001347000.1:p.Met98Val
CA149184177
NM_001360071.2:c.292A>G