Allele Registry

Canonical Allele Identifier: PA2825649186

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV001172686

ClinVar Variation:

916787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Asp210His	CA338437843 NM_001127660.2:c.628G>C