Canonical Allele Identifier: PA2825649422
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193898
ClinVar RCV Id: RCV000595105 RCV002517672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala383Val
CA239603
NM_001127660.2:c.1148C>T