Canonical Allele Identifier: PA2825649719
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350566
ClinVar RCV Id: RCV002041959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Phe665Leu
CA599295
NM_001127660.2:c.1995T>G
CA338451392
NM_001127660.2:c.1993T>C
CA338451400
NM_001127660.2:c.1995T>A