Canonical Allele Identifier: PA2829612792
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 961502
ClinVar RCV Id: RCV001235200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005661.1:p.Arg207Cys
CA149184183
NM_005670.4:c.619C>T