Canonical Allele Identifier: PA2741948185
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2916039
ClinVar RCV Id: RCV003745229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Leu724Val
CA338453290
NM_014874.4:c.2170C>G