Allele Registry

Canonical Allele Identifier: PA2825649439

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000174373

RCV000711269

RCV001084819

RCV001173689

RCV002336421

RCV004417035

ClinVar Variation:

194091

3125715

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Met393Ile	CA302734 NM_001127660.2:c.1179G>A CA599042 NM_001127660.2:c.1179G>C CA338444818 NM_001127660.2:c.1179G>T