Allele Registry

Canonical Allele Identifier: PA2827913249

Gene: MME HGNC NCBI

ClinVar RCV:

RCV000891593

ClinVar Variation:

718611

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341572.1:p.Gly225Ala	CA2675238 NM_001354643.1:c.674G>C