Canonical Allele Identifier: PA2825649387
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Thr362Pro
CA10584102
NM_001127660.2:c.1084A>C