Allele Registry

Canonical Allele Identifier: PA2825649385

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000485629

ClinVar Variation:

418294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.His361Arg	CA16616966 NM_001127660.2:c.1082A>G