Canonical Allele Identifier: PA2825649059
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg104Leu
CA320635
NM_001127660.2:c.311G>T