Canonical Allele Identifier: PA2825649744
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Leu699_Cys700del
CA2573130667
NM_001127660.2:c.2096_2101del