Canonical Allele Identifier: PA2825649343
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 843133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala317Gly
CA338441986
NM_001127660.2:c.950C>G