Allele Registry

Canonical Allele Identifier: PA915970300

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000986245

ClinVar Variation:

801444

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Arg280Pro	CA338441499 NM_014874.4:c.839G>C