Canonical Allele Identifier: PA252147
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Trp740Ser
CA252145
NM_014874.4:c.2219G>C