Canonical Allele Identifier: PA252171
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg468His
CA252169
NM_014874.4:c.1403G>A