Allele Registry

Canonical Allele Identifier: PA2829673897

Gene: MME HGNC NCBI

ClinVar RCV:

RCV001198856

RCV001797160

RCV001824932

ClinVar Variation:

931880

HGVS (amino-acid)	Matching Registered Transcripts
NP_009219.2:p.Gly579Ser	CA2675612 NM_007288.3:c.1735G>A