Allele Registry

Canonical Allele Identifier: PA2825649519

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000626228

ClinVar Variation:

523025

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Arg476Gly	CA338446686 NM_001127660.2:c.1426C>G