Allele Registry

Canonical Allele Identifier: PA645435827

Gene: MME HGNC NCBI

ClinVar RCV:

RCV000234863

RCV001814126

ClinVar Variation:

242839

HGVS (amino-acid)	Matching Registered Transcripts
NP_000893.2:p.Cys621Arg	CA10584007 NM_000902.5:c.1861T>C