Allele Registry

Canonical Allele Identifier: PA915991561

Gene: MME HGNC NCBI

ClinVar RCV:

RCV000891593

ClinVar Variation:

718611

HGVS (amino-acid)	Matching Registered Transcripts
NP_009220.2:p.Gly225Ala	CA2675238 NM_007289.4:c.674G>C