Canonical Allele Identifier: PA916047118
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 462932
ClinVar RCV Id: RCV000525708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355060.1:p.Pro76Ala
CA366191121
NM_001368131.1:c.226C>G