Canonical Allele Identifier: PA115474
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Thr206Ile
CA115472
NM_014874.4:c.617C>T