Allele Registry

Canonical Allele Identifier: PA915970235

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000790021

ClinVar Variation:

637727

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Asn252Lys	CA338439136 NM_014874.4:c.756C>A CA338439138 NM_014874.4:c.756C>G