Canonical Allele Identifier: PA103061
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg94Gln
CA252142
NM_001127660.2:c.281G>A