Canonical Allele Identifier: PA891847559
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 566249
ClinVar RCV Id: RCV000686011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg247Cys
CA598913
NM_014874.4:c.739C>T