Canonical Allele Identifier: PA645435827
Gene: MME HGNC NCBI

Linked Data

ClinVar Variation Id: 242839
ClinVar RCV Id: RCV000234863 RCV001814126
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Amino-acid Alleles

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