Canonical Allele Identifier: PA2825649048
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045318
ClinVar RCV Id: RCV001349707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg95Lys
CA338462186
NM_001127660.2:c.284G>A