Allele Registry

Canonical Allele Identifier: PA2825649135

Gene: MFN2 HGNC NCBI

ClinVar Allele:

213788

ClinVar RCV:

RCV000201063

RCV000235729

RCV000653851

RCV003338460

ClinVar Variation:

217164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.His165Arg	CA279075 NM_001127660.2:c.494A>G