Allele Registry

Canonical Allele Identifier: PA2827913055

Gene: MME HGNC NCBI

ClinVar Variation Id: 931880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341571.1:p.Gly579Ser	CA2675612 NM_001354642.2:c.1735G>A