Canonical Allele Identifier: PA2827913252
Gene: MME HGNC NCBI

Linked Data

ClinVar Variation Id: 1329740
ClinVar RCV Id: RCV001800048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341572.1:p.Tyr232Cys
CA2675241
NM_001354643.1:c.695A>G