Canonical Allele Identifier: PA252153
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg280His
CA252151
NM_014874.4:c.839G>A