Allele Registry

Canonical Allele Identifier: PA658662806

Gene: MFN2 HGNC NCBI

ClinVar Variation Id: 476771

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Ser106Arg	CA338433816 NM_014874.4:c.316A>C CA338433852 NM_014874.4:c.318C>A CA338433854 NM_014874.4:c.318C>G