Canonical Allele Identifier: PA2825649050
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg95Gly
CA16609877
NM_001127660.2:c.283A>G