Allele Registry

Canonical Allele Identifier: PA2825649139

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV001236164

ClinVar Variation:

962325

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121132.1:p.His165Pro	CA338436256 NM_001127660.2:c.494A>C