Canonical Allele Identifier: PA658810027
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543230
ClinVar RCV Id: RCV000653935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Glu308Lys
CA338441876
NM_014874.4:c.922G>A