Canonical Allele Identifier: PA2825649237
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214641
ClinVar RCV Id: RCV000195514 RCV000690762 RCV000857099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.His242Arg
CA319860
NM_001127660.2:c.725A>G