Canonical Allele Identifier: PA2825649399
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Glu370Gln
CA323742
NM_001127660.2:c.1108G>C