Allele Registry

Canonical Allele Identifier: PA2825649260

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV003484473

ClinVar Variation:

2683864

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Asn252Asp	CA338439127 NM_001127660.2:c.754A>G