Canonical Allele Identifier: PA916047123
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 531807
ClinVar RCV Id: RCV000638321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355060.1:p.Met98Val
CA149184177
NM_001368131.1:c.292A>G