Canonical Allele Identifier: PA645407388
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Thr362Arg
CA16609879
NM_014874.4:c.1085C>G