Canonical Allele Identifier: PA2825649354
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala328Thr
CA18010145
NM_001127660.2:c.982G>A