Allele Registry

Canonical Allele Identifier: PA2825649117

Gene: MFN2 HGNC NCBI

ClinVar Allele:

390792

ClinVar RCV:

RCV000474635

ClinVar Variation:

408324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Gly150Val	CA16609865 NM_001127660.2:c.449G>T