Canonical Allele Identifier: PA2827912886
Gene: MME HGNC NCBI

Linked Data

ClinVar Variation Id: 1329740
ClinVar RCV Id: RCV001800048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341571.1:p.Tyr232Cys
CA2675241
NM_001354642.2:c.695A>G