Canonical Allele Identifier: PA2825649698
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 810632
ClinVar RCV Id: RCV001030783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Lys655Glu
CA338451160
NM_001127660.2:c.1963A>G