Canonical Allele Identifier: PA915969962
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg104Gln
CA338462489
NM_014874.4:c.311G>A