Canonical Allele Identifier: PA2825649183
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 568869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Glu208Asp
CA338437816
NM_001127660.2:c.624G>C
CA338437817
NM_001127660.2:c.624G>T