Allele Registry

Canonical Allele Identifier: PA915969903

Gene: MFN2 HGNC NCBI

ClinVar Variation Id: 637311

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Gln74Arg	CA338461803 NM_014874.4:c.221A>G