Allele Registry

Canonical Allele Identifier: PA103138

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000002360

RCV000789417

ClinVar Variation:

2272

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.Pro251Ala	CA252154 NM_001127660.2:c.751C>G