Allele Registry

Canonical Allele Identifier: PA645407347

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000235092

ClinVar Variation:

243073

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Val160Gly	CA10584072 NM_014874.4:c.479T>G