Canonical Allele Identifier: PA645407385
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422500
ClinVar RCV Id: RCV000486402 RCV000857101 RCV001856863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Gln360Glu
CA16616965
NM_014874.4:c.1078C>G