Canonical Allele Identifier: PA2828283997
Gene: EPM2A HGNC NCBI

Linked Data

ClinVar Variation Id: 654471
ClinVar RCV Id: RCV000810440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355058.1:p.Trp11Cys
CA4035147
NM_001368129.2:c.33G>T
CA366191564
NM_001368129.2:c.33G>C