Canonical Allele Identifier: PA105334
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005661.1:p.Gly279Ser
CA252542
NM_005670.4:c.835G>A