Canonical Allele Identifier: PA2825215951
Gene: MME HGNC NCBI

Linked Data

ClinVar Variation Id: 931880
ClinVar RCV Id: RCV001198856 RCV001797160 RCV001824932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000893.2:p.Gly579Ser
CA2675612
NM_000902.5:c.1735G>A