Allele Registry

Canonical Allele Identifier: PA1139721508

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV001174303

ClinVar Variation:

917366

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Ile253Phe	CA338439144 NM_014874.4:c.757A>T