Canonical Allele Identifier: PA314489
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 205428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005661.1:p.Arg207His
CA314488
NM_005670.4:c.620G>A