Allele Registry

Canonical Allele Identifier: PA915970032

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000789403

ClinVar Variation:

637309

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.His165Leu	CA338436259 NM_014874.4:c.494A>T