Allele Registry

Canonical Allele Identifier: PA2827913227

Gene: MME HGNC NCBI

ClinVar RCV:

RCV000239627

ClinVar Variation:

253194

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341572.1:p.Cys143Tyr	CA10586232 NM_001354643.1:c.428G>A