Allele Registry

Canonical Allele Identifier: PA2825649063

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000790011

ClinVar Variation:

637719

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Thr105Arg	CA338433802 NM_001127660.2:c.314C>G