Allele Registry

Canonical Allele Identifier: PA1139721381

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV001172686

ClinVar Variation:

916787

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Asp210His	CA338437843 NM_014874.4:c.628G>C