Canonical Allele Identifier: PA645407455
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430101
ClinVar RCV Id: RCV000492878 RCV001856973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Glu744Gly
CA338454350
NM_014874.4:c.2231A>G