Canonical Allele Identifier: PA2825649388
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Thr362Met
CA129423
NM_001127660.2:c.1085C>T