Canonical Allele Identifier: PA2825649704
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg659Lys
CA325269
NM_001127660.2:c.1976G>A