Allele Registry

Canonical Allele Identifier: PA645407386

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000485629

ClinVar Variation:

418294

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.His361Arg	CA16616966 NM_014874.4:c.1082A>G