Allele Registry

Canonical Allele Identifier: PA2825649187

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000478137

ClinVar Variation:

420142

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Asp210Tyr	CA16616963 NM_001127660.2:c.628G>T