Allele Registry

Canonical Allele Identifier: PA645435821

Gene: MME HGNC NCBI

ClinVar RCV:

RCV000239627

ClinVar Variation:

253194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000893.2:p.Cys143Tyr	CA10586232 NM_000902.5:c.428G>A