Allele Registry

Canonical Allele Identifier: PA658810092

Gene: MFN2 HGNC NCBI

ClinVar Allele:

515042

ClinVar RCV:

RCV000653890

ClinVar Variation:

543203

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Ala738Thr	CA338453821 NM_014874.4:c.2212G>A