Allele Registry

Canonical Allele Identifier: PA658827861

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000658491

RCV001855377

ClinVar Variation:

546587

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Leu76Arg	CA598778 NM_014874.4:c.227T>G