Canonical Allele Identifier: PA2825649319
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2171829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Gln296Arg
CA598957
NM_001127660.2:c.887A>G