Allele Registry

Canonical Allele Identifier: PA915991558

Gene: MME HGNC NCBI

ClinVar RCV:

RCV000239627

ClinVar Variation:

253194

HGVS (amino-acid)	Matching Registered Transcripts
NP_009220.2:p.Cys143Tyr	CA10586232 NM_007289.4:c.428G>A