Canonical Allele Identifier: PA279077
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.His165Arg
CA279075
NM_014874.4:c.494A>G