Allele Registry

Canonical Allele Identifier: PA2825649405

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000790031

ClinVar Variation:

637737

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Met376Leu	CA338443159 NM_001127660.2:c.1126A>C CA338443169 NM_001127660.2:c.1126A>T